XYY syndrome explained
|
Synonyms: | 47,XYY |
Field: | Medical genetics |
Symptoms: | None, being taller than the parents, Mildly unusual physical features, severe acne, poor coordination, weak muscle tone, learning and speech problems |
Onset: | At conception[1] |
Duration: | Lifelong |
Causes: | Two Y chromosomes in males |
Diagnosis: | Genetic testing |
Differential: | Klinefelter syndrome, Marfan syndrome, Sotos syndrome |
Prevention: | None |
Treatment: | Speech therapy, tutoring |
Prognosis: | Normal life expectancy |
Frequency: | ~1 in 1,000 males |
XYY syndrome, also known as Jacobs syndrome, is an aneuploid genetic condition in which a male has an extra Y chromosome. There are usually few symptoms.[2] These may include being taller than average and an increased risk of learning disabilities.[2] The person is generally otherwise normal, including typical rates of fertility.
The condition is generally not inherited but rather occurs as a result of a random event during sperm development. Diagnosis is by a chromosomal analysis, but most of those affected are not diagnosed within their lifetime.[2] There are 47 chromosomes, instead of the usual 46, giving a 47,XYY karyotype.
Treatment may include speech therapy or extra help with schoolwork, however outcomes are generally positive.[2] The condition occurs in about 1 in 1,000 male births.[3] Many people with the condition are unaware that they have it.[4] The condition was first described in 1961.[5]
Signs and symptoms
Physical traits
People with the 47,XYY karyotype have an increased growth rate from early childhood, with an average final height approximately 7cm (03inches) above expected final height.[6] In Edinburgh, Scotland, eight 47,XYY boys born 1967–1972 and identified in a newborn screening programme had an average height of 188.1abbr=onNaNabbr=on at age 18—their fathers' average height was 174.1abbr=onNaNabbr=on, their mothers' average height was 162.8abbr=onNaNabbr=on.[7] The increased gene dosage of three X/Y chromosome pseudoautosomal region (PAR1) SHOX genes has been postulated as a cause of the increased stature seen in all three sex chromosome trisomies: 47,XXX, 47,XXY, and 47,XYY.[8] Severe acne was noted in a very few early case reports, but dermatologists specializing in acne now doubt the existence of a relationship with 47,XYY.[9]
Prenatal testosterone levels are normal in 47,XYY males.[10] Most 47,XYY males have normal sexual development and have normal fertility.[11] [12]
Cognitive and behavioral traits
In contrast to the other common sex chromosome aneuploidies—47,XXX and 47,XXY (Klinefelter syndrome)—the average of the IQ scores of 47,XYY boys identified by newborn screening programs was not reduced compared to the general population.[13] [14] In a summary of six prospective studies of 47,XYY boys identified by newborn screening programmes, twenty-eight 47,XYY boys had an average 100.76 verbal IQ, 108.79 performance IQ, and 105.00 full-scale IQ.[15] In a systematic review including two prospective studies of 47,XYY boys identified by newborn screening programs and one retrospective study of 47,XYY men identified by screening men over 184abbr=onNaNabbr=on in height, forty-two 47,XYY boys and men had an average 99.5 verbal IQ and 106.4 performance IQ.[14] [16] [17] [18]
In prospective studies of 47,XYY boys identified by newborn screening programs, the IQ scores of 47,XYY boys were usually slightly lower than those of their siblings.[19] In Edinburgh, fifteen 47,XYY boys with siblings identified in a newborn screening program had an average 104.0 verbal IQ and 106.7 performance IQ, while their siblings had an average 112.9 verbal IQ and 114.6 performance IQ.[16]
Approximately half of 47,XYY boys identified by newborn screening programs had learning difficulties—a higher proportion than found among siblings and above-average-IQ control groups.[12] In Edinburgh, 54% of 47,XYY boys (7 of 13) identified in a newborn screening program received remedial reading teaching compared to 18% (4 of 22) in an above-average-IQ control group of 46,XY boys matched by their father's social class.[16] In Boston, USA 55% of 47,XYY boys (6 of 11) identified in a newborn screening program had learning difficulties and received part-time resource room help compared to 11% (1 of 9) in an above-average-IQ control group of 46,XY boys with familial balanced autosomal chromosome translocations.[17]
Developmental delays and behavioral problems are also found, but these characteristics vary widely among affected boys and men, are not unique to 47,XYY and are managed no differently from in 46,XY males. Aggression is not seen more frequently in 47,XYY males.
Patients with Jacobs syndrome have been shown to have a higher risk of developing certain diseases such as asthma, seizure problems, and tremors. Some 47,XYY patients have been found to have genitourinary malformations. These include cryptorchidism, hypoplastic scrotum, microphallus, and hypospadias.[20] These men could be diagnosed with infertility as a result of oligospermia or sperm chromosomal abnormalities. According to certain psychological studies, people with XYY syndrome may have problems with impulse control and emotional regulation. Increased testosterone levels were found to be correlated with an increased risk of aggressive behavior in incarcerated males with 47,XYY syndrome.[20] 47,XYY is not inherited; it usually occurs as a random event during the formation of sperm cells. An incident in chromosome separation during anaphase II (of meiosis II) called nondisjunction can result in sperm cells with an extra copy of the Y-chromosome. If one of these atypical sperm cells contributes to the genetic makeup of a child, the child will have an extra Y-chromosome in each of the body's cells.[21]
In some cases, the extra Y-chromosome results from nondisjunction during mitosis in early embryonic development. This can produce 46,XY/47,XYY mosaics.[21]
Diagnosis
47,XYY syndrome is not usually diagnosed until learning issues are present. The syndrome is diagnosed in an increasing number of children prenatally by amniocentesis and chorionic villus sampling[22] in order to obtain a chromosome karyotype, where the abnormality can be observed.
It is estimated that only 15–20% of children with 47,XYY syndrome are ever diagnosed. Of these, approximately 30% are diagnosed prenatally. For the rest of those diagnosed after birth, around half are diagnosed during childhood or adolescence after developmental delays are observed. The rest are diagnosed after any of a variety of symptoms, including fertility problems (5%)[23] have been seen.
Epidemiology
Around 1 in 1,000 boys are born with a 47,XYY karyotype. The incidence of 47,XYY is not known to be affected by the parents' ages.
History
1960s
In April 1956, Hereditas published the discovery by cytogeneticists Joe Hin Tjio and Albert Levan at Lund University in Sweden that the normal number of chromosomes in diploid human cells was 46—not 48, as had been believed for the preceding thirty years.[24] In the wake of the establishment of the normal number of human chromosomes, 47,XYY was the last of the common sex chromosome aneuploidies to be discovered, two years after the discoveries of 47,XXY,[25] 45,X[26] and 47,XXX[27] in 1959. Even the much less common 48,XXYY[28] had been discovered in 1960, a year before 47,XYY.
Screening for those X chromosome aneuploidies was possible before the advent of human chromosome analysis by noting the presence or absence of "female" sex chromatin bodies (Barr bodies) in the nuclei of interphase cells in buccal smears, a technique developed a decade before the first reported sex chromosome aneuploidy.[29] An analogous technique to screen for Y-chromosome aneuploidies by noting supernumerary "male" sex chromatin bodies was not developed until 1970, a decade after the first reported male sex chromosome aneuploidy.[30]
The first published report of a man with a 47,XYY karyotype was by the American cytogeneticist Avery Sandberg and his colleagues at Roswell Park Comprehensive Cancer Center (then known as Roswell Park Memorial Institute) in Buffalo, New York in 1961. It was an incidental finding in a normal 44-year-old, 6 ft. [183 cm] tall man of average intelligence who was karyotyped because he had a daughter with Down syndrome.[31] Only a dozen isolated 47,XYY cases were reported in the medical literature in the four years following the first report by Sandberg.[32]
The XYY syndrome, if named after the discoverer, should rightly be termed Sandberg syndrome and not Jacobs syndrome although the British cytogeneticist Patricia Jacobs did indeed contribute meaningly to our knowledge of XYY. In December 1965 and March 1966, Nature and The Lancet published the first preliminary reports by Jacobs and her colleagues at the MRC Human Genetics Unit at Western General Hospital in Edinburgh of a chromosome survey of 315 male patients at State Hospital in Carstairs, Lanarkshire—Scotland's only special security hospital for developmentally disabled people —that found nine patients, ages 17 to 36, averaging almost 6 ft. in height (avg. 5'11", range: 5'7" to 6'2"), had a 47,XYY karyotype, and mischaracterized them as aggressive and violent criminals.[32] [33] [34] [35] Over the next decade, almost all published XYY studies were on height-selected, institutionalized XYY males.
In January 1968 and March 1968, The Lancet and Science published the first U.S. reports of tall, institutionalized XYY males by Mary Telfer, a biochemist, and colleagues at the Elwyn Institute.[36] Telfer found five tall, developmentally disabled XYY boys and men in hospitals and penal institutions in Pennsylvania, and since four of the five had at least moderate facial acne, reached the erroneous conclusion that acne was a defining characteristic of XYY males.[36] After learning that convicted mass murderer Richard Speck had been karyotyped, Telfer not only incorrectly assumed the acne-scarred Speck was XYY, but reached the false conclusion that Speck was the archetypical XYY male—or "supermale" as Telfer referred to XYY males outside of peer-reviewed scientific journals.[37]
In April 1968, The New York Times—using Telfer as a main source—introduced the XYY genetic condition to the general public in a three-part series on consecutive days that began with a Sunday front-page story about the planned use of the condition as a mitigating factor in two murder trials in Paris[38] and Melbourne[39] —and falsely reported that Richard Speck was an XYY male and that the condition would be used in an appeal of his murder conviction.[34] [40] The series was echoed the following week by articles—again using Telfer as a main source—in Time and Newsweek,[41] and six months later in The New York Times Magazine.[42]
In December 1968, the Journal of Medical Genetics published the first XYY review article—by Willam Michael Court Brown (1918–1969),[43] director of the MRC Human Genetics Unit—which reported that he had found no overrepresentation of XYY males in nationwide chromosome surveys of prisons and hospitals for developmentally disabled and mentally ill people in Scotland, and concluded that studies confined to institutionalized XYY males may be guilty of selection bias, and that long-term longitudinal prospective studies of newborn XYY boys were needed.[32]
In May 1969, at the annual meeting of the American Psychiatric Association, Telfer and her Elwyn Institute colleagues reported that case studies of the institutionalized XYY and XXY males they had found convinced them that XYY males had been falsely stigmatized and that their behavior may not be significantly different from chromosomally normal 46,XY males.[44]
In June 1969, the National Institute of Mental Health (NIMH) Center for Studies of Crime and Delinquency held a two-day XYY conference in Chevy Chase, Maryland.[45] In December 1969, with a grant from the NIMH Center for Studies of Crime and Delinquency, cytogeneticist Digamber Borgaonkar at Johns Hopkins Hospital began a chromosome survey of (predominantly African-American) boys ages 8 to 18 in all Maryland institutions for delinquent, neglected, or mentally ill juveniles, which was suspended from February–May 1970 due to an American Civil Liberties Union (ACLU) lawsuit regarding the study's lack of informed consent.[46] [47]
In the late 1960s and early 1970s, screening of consecutive newborns for sex chromosome abnormalities was undertaken at seven centers worldwide: in Denver (Jan 1964–1974), Edinburgh (Apr 1967–Jun 1979), New Haven (Oct 1967–Sep 1968), Toronto (Oct 1967–Sep 1971), Aarhus (Oct 1969–Jan 1974, Oct 1980–Jan 1989), Winnipeg (Feb 1970–Sep 1973), and Boston (Apr 1970–Nov 1974).[48] The Boston study, led by Harvard Medical School child psychiatrist Stanley Walzer at Children's Hospital, was unique among the seven newborn screening studies in that it only screened newborn boys (non-private-ward newborn boys at the Boston Hospital for Women) and was funded in part by grants from the NIMH Center for Studies of Crime and Delinquency.[49] The Edinburgh study was led by Shirley Ratcliffe who focused her career on it and published the results in 1999.[50] [51]
1970s
In December 1969, Lore Zech at the Karolinska Institute in Stockholm first reported intense fluorescence of the A T-rich distal half of the long arm of the Y chromosome in the nuclei of metaphase cells treated with quinacrine mustard.[52] In April 1970, Peter Pearson and Martin Bobrow at the MRC Population Genetics Unit in Oxford and Canino Vosa at the University of Oxford reported fluorescent "male" sex chromatin bodies in the nuclei of interphase cells in buccal smears treated with quinacrine dihydrochloride, which could be used to screen for Y chromosome aneuploidies like 47,XYY.[53]
In December 1970, at the annual meeting of the American Association for the Advancement of Science (AAAS), its retiring president, geneticist H. Bentley Glass, cheered by the legalization of abortion in New York,[54] envisioned a future where pregnant women would be required by the government to abort XYY "sex deviants".[46] [55] Mischaracterization of the XYY genetic condition was quickly incorporated into high school biology textbooks[46] [56] and medical school psychiatry textbooks,[46] [57] where misinformation still persists decades later.[35]
In 1973, child psychiatrist Herbert Schreier at Children's Hospital told Harvard Medical School microbiologist Jon Beckwith of Science for the People that he thought Walzer's Boston XYY study was unethical; Science for the People investigated the study and, regarding the study, filed an ethics complaint with Harvard Medical School in March 1974.[35] In November 1974, Science for the People went public with their objections to the Boston XYY study in a press conference and a New Scientist article alleging inadequate informed consent, a lack of benefit (since no specific treatment was available) but substantial risk (by stigmatization with a false stereotype) to the subjects, and that the unblinded experimental design could not produce meaningful results regarding the subjects' behavior.[49] In December 1974, the Harvard Standing Committee on Medical Research issued a report supporting the Boston XYY study, and in March 1975, the faculty voted 199–35 to allow continuation of the study.[49] After April 1975, screening of newborns was discontinued—changes to informed consent procedures and pressure from additional advocacy groups, including the Children's Defense Fund, having led to the discontinuation of the last active U.S. newborn screening programs for sex chromosome abnormalities in Boston and Denver.[49]
In a paper published in New Scientist on November 14, 1974 entitled "XYY syndrome: a dangerous myth" found no link was found between having an extra Y chromosome and violent behavior. According to the paper, adolescents found to have an extra Y chromosome in a Maryland institution were chemically sterilized to attempt to maintain "normal behavior," despite this the paper found no major behavioral differences between XY and XYY individuals.[58]
In August 1976, Science published a retrospective cohort study by Educational Testing Service psychologist Herman Witkin and colleagues that screened the tallest 16% of men (over 184 cm (6'0") in height) born in Copenhagen from 1944 to 1947 for XXY and XYY karyotypes, and found an increased rate of minor criminal convictions for property crimes among sixteen XXY and twelve XYY men may be related to the lower intelligence of those with criminal convictions, but found no evidence that XXY or XYY men were inclined to be aggressive or violent.[59]
1980s and later
The March of Dimes sponsored five international conferences in June 1974, November 1977, May 1981, June 1984, and June 1989 and published articles from the conferences in book form in 1979, 1982, 1986, and 1991 from seven longitudinal prospective cohort studies on the development of over 300 children and young adults with sex chromosome abnormalities identified in the screening of almost 200,000 consecutive births in hospitals in Denver, Edinburgh, New Haven, Toronto, Aarhus, Winnipeg, and Boston from 1964 to 1975.[48] [60] These seven studies—the only unbiased studies of unselected individuals with sex chromosome abnormalities—have replaced the older, biased studies of institutionalized individuals in understanding the development of individuals with sex chromosome abnormalities.[61]
In May 1997, Nature Genetics published the discovery by Ercole Rao and colleagues of the X/Y chromosome pseudoautosomal region (PAR1) SHOX gene, haploinsufficiency of which leads to short stature in Turner syndrome (45,X).[62] It was subsequently postulated that the increased gene dosage of three SHOX genes leads to tall stature in the sex chromosome trisomies 47,XXX, 47,XXY, and 47,XYY.[8]
In July 1999, Psychological Medicine published a case-control study by Royal Edinburgh Hospital psychiatrist Michael Götz and colleagues that found an increased rate of criminal convictions among seventeen XYY men identified in the Edinburgh newborn screening study compared to an above-average-IQ control group of sixty XY men, which multiple logistic regression analysis indicated was mediated mainly through lowered intelligence.[63]
In June 2002, the American Journal of Medical Genetics published results from a longitudinal prospective cohort Denver Family Development Study led by pediatrician and geneticist Arthur Robinson,[64] which found that in fourteen prenatally diagnosed 47,XYY boys (from high socioeconomic status families), IQ scores available for six boys ranged from 100 to 147 with a mean of 120.[65] For the eleven of fourteen boys with siblings, in nine instances their siblings were stronger academically, but in one case the subject was performing equal to, and in another case superior to, his siblings.[65]
Society and culture
Some medical geneticists question whether the term "syndrome" is appropriate for this condition[66] because many people with this karyotype appear normal.[66] [67]
In popular culture
In June 1970, The XYY Man was published—the first of seven Kenneth Royce spy novels whose fictional tall, intelligent, nonviolent XYY hero was a reformed expert cat burglar recruited by British intelligence for dangerous assignments—and later adapted into a thirteen-episode British summer television series broadcast in 1976 and 1977.[68]
In other fictional television works, a January 1971 episode "By the Pricking of My Thumbs ..." of the British science fiction TV series Doomwatch featured an XYY boy expelled from school because his genetic condition led him to be falsely accused of nearly blinding another boy.[69] A November 1993 episode of the American police procedural TV series Law & Order, "Born Bad", portrays a 14-year-old XYY sociopathic murderer.[70] The May 2007 season finale episode, "Born To Kill", of the American police procedural TV series depicts a 34-year-old XYY serial killer.[71]
The false stereotype of XYY boys and men as violent criminals has also been used as a plot device in the horror films Il gatto a nove code in February 1971 (dubbed into English as The Cat o' Nine Tails in May 1971) and Alien 3 in May 1992.[34] [35] The main character of the 2005 film Neo Ned is a neo-nazi who has an extra Y chromosome.[72]
See also
External links
Notes and References
- Web site: XYY Syndrome .
- Web site: XYY Syndrome. 2012. NORD (National Organization for Rare Disorders). 11 November 2017.
- Web site: 47,XYY syndrome. Genetics Home Reference. en. 2017-03-19. January 2009.
- Web site: 47, XYY syndrome. Genetic and Rare Diseases Information Center (GARD). 11 November 2017. en. 2017. 11 November 2017. https://web.archive.org/web/20171111205247/https://rarediseases.info.nih.gov/diseases/5674/47-xyy-syndrome. dead.
- Book: Bostwick. David G.. Cheng. Liang. Urologic Surgical Pathology E-Book. 2014. Elsevier Health Sciences. 978-0-323-08619-6. 682. en.
- Web site: Nielsen, Johannes. 1998. How is height growth?. 2010-03-07. https://web.archive.org/web/20100307091453/http://www.aaa.dk/TURNER/ENGELSK/XYY.HTM#height. XYY males. An orientation . The Turner Center, Aarhus Psychiatric Hospital, Risskov, Denmark.
- Ratcliffe. Shirley G.. Pan. Huiqi. McKie. Mark. November–December 1992. Growth during puberty in the XYY boy. Annals of Human Biology. 19. 6. 579–587. 10.1080/03014469200002392. 1476413.
- Book: Cohen, Pinchas . Shim, Melanie . 2007 . Hyperpituitarism, tall stature, and overgrowth syndromes . Kliegman, Robert M. . Behrman, Richard E. . Jenson, Hal B. . Stanton, Bonita F. . Nelson textbook of pediatrics . 18th . Philadelphia . . 978-1-4160-2450-7 . 2303–2307. p. 2304: Table 561-1. Differential diagnosis of tall stature and overgrowth syndromes. Postnatal overgrowth leading to childhood tall stature—includes: Klinefelter syndrome (XXY), SHOX excess syndromes, XYY.
- Kanaka-Gantenbein, Christina . Kitsiou, Sophia . Mavrou, Ariadni . Stamoyannou, Lela . Kolialexi, Aggeliki . Kekou, Kyriaki . Liakopoulou, Magda . Chrousos, George . April 2004 . Tall stature, insulin resistance, and disturbed behavior in a girl with the triple X syndrome harboring three SHOX genes: offspring of a father with mosaic Klinefelter syndrome but with two maternal X chromosomes . . 61 . 5 . 205–210 . 10.1159/000076532 . 14752208. 41958098 .
- Aksglaede, Lise . Skakkebaek, Niels E. . Juul, Anders . January 2008 . Abnormal sex chromosome constitution and longitudinal growth: serum levels of insulin-like growth factor (IGF)-I, IGF binding protein-3, luteinizing hormone, and testosterone in 109 males with 47,XXY, 47,XYY, or sex-determining region of the Y chromosome (SRY)-positive 46,XX karyotypes . . 93 . 1 . 169–176 . 10.1210/jc.2007-1426 . 17940117 . https://ghostarchive.org/archive/20221009/http://jcem.endojournals.org/cgi/reprint/93/1/169.pdf . 2022-10-09 . live. free .
- Tüttelmann, Frank . Gromoll, Jörg . 2010 . Novel genetic aspects of Klinefelter's syndrome . Mol Hum Reprod . 16. 6. 386–95. 10.1093/molehr/gaq019 . 20228051. free .
- Book: Plewig, Gerd . Kligman, Albert M. . 2000 . Acne and rosacea . 3rd . 377 . Philadelphia . . 978-3-540-66751-3.
- Ratcliffe, Shirley G. . Read, Graham . Pan, Huiqi . Fear, Claudine . Lindenbaum, Richard . Crossley, Jennifer . September 1994 . Prenatal testosterone levels in XXY and XYY males . . 42 . 3 . 106–109 . 7995613 . 10.1159/000184157.
- Book: Gardner, R.J. McKinlay . Sutherland, Grant R. . 2004 . Chromosome abnormalities and genetic counseling . 3rd . 29–30, 42, 199, 207, 257, 263, 393, 424–430 . Oxford . . 978-0-19-514960-9 . From early meiotic studies, it was concluded that the extra Y was eliminated before the spermatocyte formed, with an X-Y bivalent usually seen at diakinesis, and more recent studies support this concept. However, FISH analyses of sperm, enabling hundreds of cells to be analyzed, have shown a very small increased faction of 24,YY spermatozoa in the ejaculate of XYY men (Table 12-1). Thus it appears the vast majority of spermatocytes lose the extra Y before entering meiosis, a very few XYY primary spermatocytes are able to slip through and produce YY (and XY) spermatozoa. These cytogenetic findings parallel the observation that XYY men have no discernible increase in risk to have children with a sex chromosome abnormality. A true increased risk of a fraction of a per cent could be distinguished only with the greatest of difficulty when the background population risk is of a similar order of magnitude. As for the autosomes, no convincing case exists for any increased risk for aneuploidy in the children of men with 47,XYY.
To our knowledge, there is no report of a discernibly increased risk for the XYY male to have chromosomally abnormal children. A slight increase in gonosomal imbalances in sperm (Table 12-1) might nevertheless lead some to choose prenatal diagnosis..
- Book: Gardner, R.J. McKinlay . Sutherland, Grant R. . Shaffer, Lisa G. . 2012. Chromosome abnormalities and genetic counseling. 4th. Oxford. Oxford University Press. 978-0-19-537533-6. 9–10, 12, 36, 52, 221, 224, 230, 285–286, 293, 440–441, 477–480, 484. The two other conditions, XXX and XYY, apparently have little effect on fertility; furthermore, they are not discernibly associated with any increased risk for chromosomally abnormal offspring.
While the IQ is in the normal range, it is usually lower than those of sibs or controls, and about half of XYY boys have a mild learning difficulty, and may display poor attention and impulsivity in the classroom..
- Book: Bender. Bruce G.. Puck. Mary H.. Salbenblatt. James A.. Robinson. Arthur. 1986. Cognitive development of children with sex chromosome abnormalities. Smith. Shelley D.. Genetics and learning disabilities. San Diego. College-Hill Press. 175–201. 978-0-88744-141-7. Figure 8-3. Estimated full-scale IQ distributions for SCA and control children: 47,XXX (mean ~83), 45,X & Variant (mean ~85), 47,XXY (mean ~95), 47,XYY (mean ~100), Controls and SCA Mosaics (mean ~104). https://archive.org/details/geneticslearning0000unse/page/175.
- Leggett. Victoria. Jacobs. Patricia. Nation. Kate. Scerif. Gaia. Bishop. Dorothy V. M.. February 2010. Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review. Dev Med Child Neurol. 52. 2. 119–129. 10.1111/j.1469-8749.2009.03545.x. 2820350. 20059514. Males with XYY have average IQs, consistent with the one study showing normal brain volume on magnetic resonance imaging. In contrast, both XXY and XXX groups tend to have below-average verbal IQ and small cerebral volume..
- Book: Netley, Charles T.. 1986. Summary overview of behavioural development in individuals with neo-natally identified X and Y aneuploidy. Ratcliffe, Shirley G. . Paul, Natalie . Prospective studies on children with sex chromosome aneuploidy. Birth defects original article series 22 (3). 293–306. New York. Alan R. Liss. 978-0-8451-1062-1.
- Book: Ratcliffe, Shirley G.. 1994. The psychological and psychiatric consequences of sex chromosome abnormalities in children, based on population studies. Poustka. Fritz . Basic approaches to genetic and molecularbiological developmental psychiatry. Berlin. Quintessenz. 99–122. 978-3-86128-209-9. 19 XYY boys: average verbal IQ=100.2 (range 66–121), average performance IQ=104.3 (range 83–131), average full-scale IQ=102.3; 86 XY control boys matched by the 1970 Registrar General's Classification of Social Class based on their father's occupation: average full-scale IQ=116.1;
15 XYY boys with siblings: average verbal IQ=104.0, average performance IQ=106.7; siblings of XYY boys: average verbal IQ=112.9, average performance IQ=114.6..
- Book: Walzer. Stanley. Bashir. Anthony S. Silbert. Annette R.. 1991. Cognitive and behavioral factors in the learning disabilities of 47,XXY and 47,XYY boys. Evans. Jane A. Hamerton. John L. Robinson. Arthur . Children and young adults with sex chromosome aneuploidy: follow-up, clinical and molecular studies. Birth defects original article series 26 (4). 45–58. New York. Wiley-Liss. 978-0-471-56846-9. 11 XYY boys: average verbal IQ=103.96 (range=73–139), average performance IQ=106.64 (range=84–129), average full-scale IQ=105.45 (range=80–138); 9 XY familial balanced autosomal chromosome translocation control boys: average full-scale IQ=119.33 (range=103–137)..
- Theilgaard. Alice. December 1984. A psychological study of the personalities of XYY- and XXY-men. Results. Acta Psychiatr Scand Suppl. 70. s315. 38–49. 10.1111/j.1600-0447.1984.tb11065.x. 6595938. 221445990. 12 XYY men over 184 cm tall: average verbal IQ=99.9, average performance IQ=97.8, average full-scale IQ=99.1 (range: 77–124); 12 XY control men over 184 cm tall, matched by age, height, and social class based on their father's occupation: average full-scale IQ=119.4.
- Book: Robinson. Arthur. Bender. Bruce G.. Puck. Mary H.. Salbenblatt. James A.. 1985. Growth and development of children with a 47,XYY karyotype. Sandberg. Avery A. . The Y chromosome: Part B. Clinical aspects of Y chromosome abnormalities. Progress and topics in cytogenetics 6. New York. Alan R. Liss. 265–275. 978-0-8451-2498-7. 12557546. Follow-up studies on the total unselected group of prepubertal or early pubertal 47,XYY boys are remarkably similar despite different methods of following their progress and different policies of informing the parents. As with other forms of SCA there is great variability in the expression of the genotype. The most consistent findings are height over the 50th percentile, normal IQ usually a little lower than that of sibling controls, delay in speech and language development, and the need for extra help in school..
- Bardsley . Martha Zeger . Kowal . Karen . Levy . Carly . Gosek . Ania . Ayari . Natalie . Tartaglia . Nicole . Lahlou . Najiba . Winder . Breanna . Grimes . Shannon . Ross . Judith L. . 47,XYY Syndrome: Clinical Phenotype and Timing of Ascertainment . The Journal of Pediatrics . October 2013 . 163 . 4 . 1085–1094 . 10.1016/j.jpeds.2013.05.037. 23810129 . 4097881 .
- Robinson, David O. . Jacobs, Patricia A. . November 1, 1999 . The origin of the extra Y chromosome in males with a 47,XYY karyotype . . 8 . 12 . 2205–2209 . 10545600 . 10.1093/hmg/8.12.2205. free .
- Book: NORD Guide to Rare Disorders. National Organization for Rare Disorders. 2003. Lippincott Williams & Wilkins. 978-0-7817-3063-1. 91. en.
- Book: Davis, Andrew S. . Psychopathology of Childhood and Adolescence: A Neuropsychological Approach. 2012-12-20. Springer Publishing Company. 978-0-8261-0928-6. 586. en.
- 10.1111/j.1601-5223.1956.tb03010.x . Tjio, Joe Hin . Levan, Albert . April 1956 . The chromosome number of man . . 42 . 1 . 1–6. 10261/15776 . free .
- Jacobs, Patricia A. . Strong, John A. . January 31, 1959 . A case of human intersexuality having a possible XXY sex-determining mechanism . . 183 . 4657 . 302–3 . 10.1038/183302a0 . 13632697. 1959Natur.183..302J . 38349997 .
- Ford, Charles E. . Jones, Kenneth W. . Polani, Paul E. . de Almeida, José Carlos Cabral . Briggs, John H. . April 4, 1959 . A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome) . . 273 . 7075 . 711–3 . 10.1016/S0140-6736(59)91893-8 . 13642858.
- Jacobs, Patricia A. . Baikie, Albert G. . Court Brown, W. Michael . MacGregor, Thomas N. . Harnden, David G. . September 26, 1959 . Evidence for the existence of the human "super female" . . 274 . 7100 . 423–5 . 10.1016/S0140-6736(59)90415-5 . 14406377.
- Muldal, Sylfest . Ockey, Charles H. . August 27, 1960 . The "double male": a new chromosome constitution in Klinefelter's syndrome . . 276 . 7147 . 492–3 . 10.1016/S0140-6736(60)91624-X.
- Barr, Murray L. . Bertram, Ewart G. . April 30, 1949 . A morphological distinction between neurones of the male and female, and the behaviour of the nucleolar satellite during accelerated nucleoprotein synthesis . . 163 . 4148 . 676–677 . 10.1038/163676a0 . 18120749 . 1949Natur.163..676B . 4093883 .
- June 6, 1970 . In pursuit of the Y chromosome . . 226 . 5249 . 897 . 10.1038/226897a0 . 4192294. 1970Natur.226..897. . 4169027 . free .
- February 6, 1971 . Dyeing the Y chromosome . . 297 . 7693 . 275–276 . 10.1016/S0140-6736(71)91008-7.
- Sandberg, Avery A. . Koepf, George F. . Ishihara, Takaaki . Hauschka, Theodore S. . August 26, 1961 . An XYY human male . . 278 . 7200 . 488–489 . 13746118 . 10.1016/S0140-6736(61)92459-X.
- Hauschka, Theodore S. . Hasson, John E. . Goldstein, Milton N. . Koepf, George F. . Sandberg, Avery A. . March 1962 . An XYY man with progeny indicating familial tendency to non-disjunction . . 14 . 22–30 . 13905424 . 1932182 . 1.
- Court Brown . W. Michael . December 1968 . Males with an XYY sex chromosome complement . J Med Genet. 5 . 4 . 341–59 . 10.1136/jmg.5.4.341 . 4890326 . 1468679.
- Jacobs, Patricia A. . Brunton, Muriel . Melville, Marie M. . Brittain, Robert P. . McClemont, William F. . December 25, 1965 . Aggressive behavior, mental sub-normality and the XYY male . . 208 . 5017 . 1351–2 . 10.1038/2081351a0 . 5870205. 1965Natur.208.1351J . 4145850 .
- Price, William H. . Strong, John A. . Whatmore, Peter B. . McClemont, William F. . March 12, 1966 . Criminal patients with XYY sex-chromosome complement . . 287 . 7437 . 565–6 . 10.1016/S0140-6736(66)90760-4 . 4159988.
- editorial . March 12, 1966 . The YY syndrome . . 287 . 7437 . 583–4 . 10.1016/S0140-6736(66)90771-9 . 4159658.
- Price, William H. . Whatmore, Peter B. . February 25, 1967 . Criminal behavior and the XYY male . . 213 . 5078 . 815 . 10.1038/213815a0 . 6031815. 1967Natur.213..815P . 4158233 . free .
- Price, William H. . Whatmore, Peter B. . March 4, 1967 . Behaviour disorders and pattern of crime among XYY males identified at a maximum security hospital . . 1 . 5539 . 533–6 . 6017153 . 1841401 . 10.1136/bmj.1.5539.533.
- Court Brown, W. Michael . Price, William H. . Jacobs, Patricia A. . May 11, 1968 . Further information on the identity of 47,XYY males . . 2 . 5601 . 325–8 . 5689727 . 1985597 . 10.1136/bmj.2.354.325-a.
- Jacobs, Patricia A. . Price, William H. . Court Brown, W. Michael . Brittain, Robert P. . Whatmore, Peter B. . May 1968 . Chromosome studies on men in a maximum security hospital . . 31 . 4 . 339–58 . 10.1111/j.1469-1809.1968.tb00566.x . 83969793 .
- Court Brown, W. Michael . Price, William H. . Jacobs, Patricia A. . November 23, 1968 . The XYY male . . 4 . 5629 . 513 . 10.1136/bmj.4.5629.513-a . 62593088 .
- Jacobs, Patricia A. . September 1982 . The William Allan Memorial Award address: human population cytogenetics: the first twenty-five years . Am J Hum Genet. 34 . 5 . 689–98 . 6751075 . 1685430.
- Book: Harper, Peter S. . 2006 . The sex chromosomes . First years of human chromosomes : the beginnings of human cytogenetics . Bloxham . Scion . 978-1-904842-24-8 . 77–96.
- Book: Green, Jeremy . 1985 . Media sensationalism and science: The case of the criminal chromosome . 139–161 . Shinn, Terry . Whitley, Richard . Expository science: Forms and functions of popularisation . 978-90-277-1831-0 . . Dordrecht, Holland . https://archive.org/details/expositoryscienc0000unse/page/139 .
- Book: Beckwith, Jonathan R. . 2002 . The myth of the criminal chromosome . Making genes, making waves: A social activist in science . https://archive.org/details/makinggenesmakin0000beck . registration . Cambridge, Mass. . . 978-0-674-00928-8 . 116–134.
- Telfer, Mary A. . Baker, David . Longtin, Lucien . January 13, 1968 . YY syndrome in an American Negro . . 291 . 7533 . 95 . 10.1016/S0140-6736(68)90107-4 . 4169701.
- Telfer, Mary A. . Baker, David . Clark, Gerald R. . Richardson, Claude E. . March 15, 1968 . Incidence of gross chromosomal errors among tall criminal American males . . 159 . 3820 . 1249–50 . 10.1126/science.159.3820.1249 . 1723887 . 5715587. 1968Sci...159.1249T . 27416349 .
- Telfer, Mary A. . November–December 1968 . Are some criminals born that way? . Think . 34 . 6 . 24–8 . 0040-6112.
- Daniel Hugon, Paris, France
- Lawrence Hannell, Melbourne, Australia
- News: October 10, 1968 . Extra chromosome brings acquittal on murder charge . . 94 .
- News: Auerbach, Stuart . October 10, 1968 . Genetic abnormality is basis for acquittal . . A1 . July 7, 2017 . October 26, 2012 . https://web.archive.org/web/20121026113916/http://pqasb.pqarchiver.com/washingtonpost_historical/access/185091562.html?FMT=ABS&FMTS=ABS:AI . dead .
- News: Getze, George . February 3, 1969 . Australia precedent for XYY syndrome case held dubious . . C1 . July 7, 2017 . January 31, 2013 . https://archive.today/20130131173103/http://pqasb.pqarchiver.com/latimes/access/673351452.html?FMT=ABS&FMTS=ABS:AI . dead . An Australian murder case that was reported to have been decided on the basis of the so-called XYY syndrome actually was not concerned with chromosome counts at all.
- News: Lyons, Richard D. . April 21, 1968 . Genetic abnormality is linked to crime; Genetics linked to violent crimes . . 1 .
- News: Lyons, Richard D. . April 22, 1968 . Ultimate Speck appeal may cite a genetic defect . . 43 .
- News: Lyons, Richard D. . April 23, 1968 . Chromosome test for flaws costly; 2 scientists cite scarcity of skilled aides for analyses . . 27 .
- News: editorial . April 23, 1968 . Nature or nurture? . . 46 .
- News: April 23, 1968 . Geneticist: Didn't test Speck . . 8.
- News: November 26, 1968 . Getty tells Speck case plea basis; 10 issues are raised regarding trial . . A16 . July 7, 2017 . October 19, 2012 . https://web.archive.org/web/20121019192904/http://pqasb.pqarchiver.com/chicagotribune/access/586226742.html?dids=586226742:586226742&FMT=ABS&FMTS=ABS:AI . dead .
- Engel, Eric . September 1972 . The making of an XYY . Am J Ment Defic. 77 . 2 . 123–7 . 5081078. —article by Vanderbilt University endocrinologist and geneticist Eric Engel, who performed two confidential chromosome analyses of Speck in September 1966 and June 1968. Based on mischaracterizations of XYY males as aggressive and violent criminals in the December 1965 and March 1966 preliminary reports by Jacobs, et al., Engel had made an unsolicited request in August 1966 to Speck's appointed defense attorney, Cook County Public Defender Gerald W. Getty, to confidentially karyotype Speck—which was repeated after false news reports in April 1968 that Speck was XYY.
- May 3, 1968 . Of chromosomes & crime . . 91 . 18 . 41 . https://web.archive.org/web/20101029122601/http://www.time.com/time/magazine/article/0,9171,841254,00.html. dead. October 29, 2010.
- May 6, 1968 . Born bad? . . 76 . 19 . 87.
- News: Stock, Robert W. . October 20, 1968 . The XYY and the criminal . . SM30 .
- The first XYY review article, by W. Michael Court Brown, a physician and world authority on radiation biology and cytogenetics, was published in December 1968. Court Brown had established the MRC Clinical Effects of Radiation Unit at Western General Hospital in Edinburgh in 1956, which was renamed the MRC Clinical and Population Cytogenetics Unit in 1967 (and subsequently renamed the MRC Human Genetics Unit in 1988). In 1962, Court Brown had been the first to suggest—based on findings of antisocial behavior in some institutionalized Klinefelter syndrome (47,XXY) patients and psychosis in some institutionalized Triple X syndrome (47,XXX) patients—that individuals with sex chromosome abnormalities could be held in law to suffer from diminished responsibility.
- Court Brown . W. Michael . September 8, 1962 . Sex chromosomes and the law . . 280 . 7254 . 508–509 . 10.1016/S0140-6736(62)90378-1.
- January 4, 1969 . William Michael Court Brown . . 293 . 7584 . 57–58 . 10.1016/S0140-6736(69)91029-0 . 4178806.
- Harnden, David G. . March 1969 . W.M. Court Brown . . 6 . 1 . 107–108 . 10.1136/jmg.6.1.107 . 4890463 . 1468708.
- Book: Hsu, T. C. . 1979 . Human and mammalian cytogenetics : an historical perspective . New York . . 978-0-387-90364-4 . 41–42 .
- News: Associated Press . May 6, 1969 . A kind word said for the XYY men; Psychiatrist cites evidence many are good citizens . . 93 .
- Clark, Gerald R. . Telfer, Mary A. . Baker, David . Rosen, Marvin . May 1970 . Sex chromosomes, crime, and psychosis . . 126 . 11 . 1659–63 . 5443650 . 10.1176/ajp.126.11.1659 . 2010-04-16 . 2011-06-12 . https://web.archive.org/web/20110612031407/http://ajp.psychiatryonline.org/cgi/content/abstract/126/11/1659 . dead .
- Baker, David . Telfer, Mary A. . Richardson, Claude E. . Clark, Gerald R. . November 2, 1970 . Chromosome errors in men with antisocial behavior. Comparison of selected men with Klinefelter syndrome and XYY chromosome pattern . . 214 . 5 . 869–78 . 4248395 . 10.1001/jama.214.5.869 .
- Book: Shah, Saleem A. . 1970 . Report on the XYY chromosomal abnormality . Chevy Chase, Md. . NIMH Center for Studies of Crime and Delinquency . Public Health Service publication No. 2103 . 235264. June 19–20, 1969 XYY conference.
- Book: Pyeritz, Reed . Schreier, Herb . Madansky, Chuck . Miller, Larry . Beckwith, Jon . 1977 . The XYY male: The making of a myth . Ann Arbor Science for the Peopleial Collective . Biology as a social weapon . 86–100 . Minneapolis . Burgess Pub. Co . 978-0-8087-4534-1.
- News: Associated Press . December 27, 1969 . Gene abnormality set for Md. study . . B7 . July 7, 2017 . October 26, 2012 . https://web.archive.org/web/20121026103520/http://pqasb.pqarchiver.com/washingtonpost_historical/access/149109532.html?FMT=ABS&FMTS=ABS:AI . dead .
- News: Bauer, Diane . January 22, 1970 . Maryland tests for criminal potential . . 7. reprinted in Katz (1972). Experimentation with human beings, pp. 342–343.
- News: Cohen, Richard M. . February 7, 1970 . Genetic study is opposed . . B2 . July 7, 2017 . October 26, 2012 . https://web.archive.org/web/20121026103532/http://pqasb.pqarchiver.com/washingtonpost_historical/access/158044782.html?FMT=ABS&FMTS=ABS:AI . dead .
- News: Bauer, Diane . February 13, 1970 . XYY tests stop . . 5. reprinted in Katz (1972). Experimentation with human beings, pp. 343–344.
- News: Bauer, Diane . May 4, 1970 . Criminal-prone tests resumed . . 1. reprinted in Katz (1972). Experimentation with human beings, p. 344.
- May 18, 1970 . Congenital criminals? . . 75 . 20 . 98–99.
- Book: Katz, Jay . Capron, Alexander Morgan . Glass, Eleanor Swift . 1972 . Experimentation with human beings; the authority of the investigator, subject, professions, and state in the human experimentation process . registration . 342–346 . New York . . 978-0-87154-438-4 .
- Book: Borgaonkar, Diagamber S. . Shah, Saleem A. . 1974 . The XYY chromosome male—or syndrome? . 135–222 . Steinberg, Arthur Gerald . Bearn, Alexander G. . Progress in medical genetics. Volume 10 . New York . Grune & Stratton . 978-0-8089-0841-8.
- Book: Borgaonkar, Diagamber S. . 1978 . Cytogenic screening of community-dwelling males . 215–234 . Cohen, Bernice H. . Lilienfield, Abraham M. . Huang, P. C. . Genetic issues in public health and medicine . Springfield, Ill. . Charles C Thomas . 978-0-398-03659-1 . https://archive.org/details/geneticissuesinp00cohe/page/215 .
- Book: Washington, Harriet A. . 2004 . Born for evil? Stereotyping the karyotype: A case history in the genetics of aggressiveness . Roelcke, Volker . Maio, Giovanni . Twentieth century ethics of human subjects research : historical perspectives on values, practices, and regulations . 319–334 . Stuttgart . . 978-3-515-08455-0.
- Book: Washington, Harriet A. . 2006 . The children's crusade: research targets young African Americans . Medical apartheid : the dark history of experimentation on black Americans from colonial times to the present . 279–283 . New York . . 978-0-385-50993-0 . https://archive.org/details/medicalapartheid00wash/page/279 .
- Book: Robinson, Arthur . Lubs, Herbert A. . Bergsma, Daniel . 1979 . Sex chromosome aneuploidy: prospective studies on children. Birth defects original article series 15 (1) . New York . . 978-0-8451-1024-9.
- Book: Stewart, Donald A. . 1982 . Children with sex chromosome aneuploidy: follow-up studies . Birth defects original article series 18 (4) . New York . . 978-0-8451-1052-2.
- Book: Ratcliffe, Shirley G. . Paul, Natalie . 1986 . Prospective studies on children with sex chromosome aneuploidy . Birth defects original article series 22 (3) . New York . . 978-0-8451-1062-1.
- Book: Evans, Jane A. . Hamerton, John L. . Robinson, Arthur . 1991 . Children and young adults with sex chromosome aneuploidy: follow-up, clinical and molecular studies . Birth defects original article series 26 (4) . New York . . 978-0-471-56846-9.
- Beckwith, Jon . King, Jonathan . November 1974 . The XYY syndrome: a dangerous myth . . 64 . 923 . 474–476 . 11664346 . 2015-07-02 . 2023-01-11 . https://web.archive.org/web/20230111211926/https://books.google.com/books?id=XAU4aZVrYv4C&pg=PA474 . dead .
- News: Brody, Jane E. . November 15, 1974 . Scientists' group terms Boston study of children with extra sex chromosome unethical and harmful . . 93 .
- News: Knox, Richard . November 16, 1974 . Scientists oppose survey of chromosome disorder . . 3 . July 7, 2017 . January 31, 2013 . https://archive.today/20130131135410/http://pqasb.pqarchiver.com/boston/access/1975367112.html?FMT=ABS&FMTS=ABS:AI . dead .
- Culliton, Barbara J. . November 22, 1974 . Patients' rights: Harvard is site of battle over X and Y chromosomes . . 186 . 4165 . 715–717 . 10.1126/science.186.4165.715 . 1739961 . 11643569. 1974Sci...186..715C .
- News: Brody, Jane E. . December 14, 1974 . Harvard backs genetic study; research involving young with XYY chromosome had been criticized . . 20 .
- News: Bruzelius, Nils . December 15, 1974 . Harvard Medical School panel rejects plea to end gene study . . 8 . July 7, 2017 . January 31, 2013 . https://archive.today/20130131215841/http://pqasb.pqarchiver.com/boston/access/2056634312.html?FMT=ABS&FMTS=ABS:AI . dead .
- Culliton, Barbara J. . December 27, 1974 . Briefing: Harvard faculty says XYY study should continue . . 186 . 4170 . 1188–1189 . 10.1126/science.186.4170.1189-b . 1739250. 17833922.
- Beckwith, Jon . Elseviers, Dirk . Gorni, Luigi . Mandansky, Chuck . Csonka, Leslie . King, Jonathan . January 31, 1975 . Harvard XYY study . . 187 . 4174 . 10.1126/science.11643259 . 11643259 . 298–9. 1975Sci...187..298B .
- News: March 15, 1975. Harvard vote backs child behavior study. The Boston Globe. 7. The Harvard Medical School faculty voted last night 199–35, to allow continuation of studies at Children's Hospital Medical Center and at Boston Hospital for Women on children with an extra sex chromosome.. July 7, 2017. January 31, 2013. https://archive.today/20130131155148/http://pqasb.pqarchiver.com/boston/access/1974822802.html?FMT=CITE&FMTS=CITE:AI. dead.
- News: Brody, Jane E. . June 20, 1975 . Babies' screening is ended in Boston; extra chromosome study stirred controversy on its ethics and value . . 6 . Dr. Walzer said that when he stopped screening on the study's fifth anniversary in April,... .
- Culliton, Barbara J. . June 27, 1975 . XYY: Harvard researcher under fire stops newborn screening . . 188 . 4195 . 1284–1285 . 10.1126/science.11643276 . 1741001 . 11643276. 1975Sci...188.1284C .
- News: Knox, Richard. July 6, 1975. XYY battle is over, research ethic war isn't. The Boston Globe. A4. In May...Walzer nevertheless decided to cut short his XYY screening by about eight months.. July 7, 2017. January 31, 2013. https://archive.today/20130131165145/http://pqasb.pqarchiver.com/boston/access/2024063982.html?FMT=ABS&FMTS=ABS:AI. dead.
- News: Weiss, Philip . September 15, 1975 . Ending the test for extra chromosomes . .
- Bauer . Diane . Bayer . Ronald . Beckwith . Jonathan . Bermant . Gordon . Borgaonkar . Digamber S. . Callahan . Daniel . Caplan . Arthur . Conrad . John . Culver . Charles M. . Dworkin . Gerald . Edgar . Harold . Gaylin . Willard . Gerald . Park . Harris . Clarence . King . Johnathan . Macklin . Ruth . Mazur . Allan . Michels . Robert . Mone . Carola . Petchesky . Rosalind . Rosalind Petchesky . Powledge . Tabitha M. . Pyeritz . Reed E. . Robinson . Arthur . Scanlon . Thomas . Shah . Saleem A. . Shannon . Thomas A. . Steinfels . Margaret . Swazey . Judith P. . Wachtel . Paul . Walzer . Stanley . August 1980 . The XYY controversy: researching violence and genetics . . 10 . 4 . Suppl 1–32 . 7399889 . 3560454 . Stanley Walzer: On the issue of informed consent prior to newborn chromosome screening, Science for the People proved correct. They had predicted that the amount of information that had to be shared prior to screening was so extensive and complex that true informed consent was impossible to obtain at that point.
Arthur Robinson: When we stopped in 1974, we had done 40,000 analyses. From an epidemiological point of view, I would have preferred to have done 80,000... Why did we stop? Well, in the first place there was the informed consent problem. When we started in 1964 feelings about informed consent were very different. Try to imagine how one would go about getting truly informed consent from 40,000 people. With the implications of what we would find, in a sex chromosome variation, it would be an almost impossible task. That's one reason why we stopped.. 10.2307/3560454 .
- Sapietis. Una. Butler. Gary. Obituary: Shirley Ratcliffe. BMJ. 21 July 2014. 349. g4716. 10.1136/bmj.g4716. 220108224.
- Web site: Archive record: Dr Shirley Ratcliffe and the Edinburgh MRC Clinical and Population Cytogenetics Unit Study of Long Term Outcomes for Children Born with Sex Chromosome Abnormalities. Wellcome Library Western Manuscripts and Archives catalogue. 27 February 2018. en.
- Zech, Lore . December 1969 . Investigation of metaphase chromosomes with DNA-binding flurochromes . . 58 . 2–3 . 463 . 10.1016/0014-4827(69)90531-X .
- Pearson, Peter L. . Bobrow, Martin . Vosa, Canio G. . April 4, 1970 . Technique for identifying Y chromosomes in human interphase nuclei . . 226 . 5240 . 78–80 . 4190810 . 10.1038/226078a0. 1970Natur.226...78P . 4013867 .
- News: Kovach, Bill . April 11, 1970 . Final approval of abortion bill voted in Albany; Rockefeller to sign it over weekend despite appeal by Cooke for veto . . 1 .
- News: Sullivan, Walter . December 29, 1970 . Growth to slow down, association head says . . 14 .
- Glass, Bentley . January 8, 1971 . Science: endless horizons or golden age? . . 171 . 3966 . 23–29 . 10.1126/science.171.3966.23 . 1731074 . 17737984. 1971Sci...171...23G .
- Glass, Bentley . April 9, 1971 . Reply to: Less than golden future . . 172 . 3979 . 111–112 . 10.1126/science.172.3979.111-c . 1730891 . 17735208.
- Glass, Bentley . July 9, 1971 . Reply to: What price the perfect baby? . . 173 . 3992 . 103–104 . 1732191 . 5104145 . 10.1126/science.173.3992.103-c .
- Book: Otto, James Howard . Towle, Albert . 1973 . Modern biology . New York . Holt, Rinehart and Winston . 978-0-03-091337-2 . 185 . Another abnormal condition results when a normal X-bearing egg is fertilized by a YY sperm, formed by non-disjunction during spermatogenesis. This produces an XYY male who is usually over six feet in height and very aggressive. .
- Book: Freedman, Alfred M. . Kaplan, Harold I. . Sadock, Benjamin J. . 1972 . Modern Synopsis of Comprehensive Textbook of Psychiatry . 1st . Baltimore . Williams & Wilkins . 1232929 . 711 . Figure 43.2.
- Book: Sadock, Benjamin James . Sadock, Virginia Alcott . 2007 . Kaplan and Sadock's Synopsis of Psychiatry : Behavioral Sciences/Clinical Psychiatry . 10th . Philadelphia . Lippincott Williams & Wilkins . 978-0-7817-7327-0 . 154 . A famous case of an "XYY" insanity defense is illustrated in Figure 4.4–1. Richard Speck. He was convicted in 1966 of slaying eight nurses in Chicago by stabbing and strangulation. His legal defense was based on his genetic makeup, which was "XYY". Individuals with these genes have been reported to be tall, mentally retarded, have acne, and show aggressive behavior... (Courtesy of Wide World Photos.).
- Web site: XYY SYNDROME - A DANGEROUS MYTH | Office of Justice Programs. www.ojp.gov.
- Witkin . Herman A. . Mednick . Sarnoff A. . Schulsinger . Fini . Bakkestrøm . Eskild . Christiansen . Karl O. . Goodenough . Donald R. . Hirschhorn . Kurt . Lundsteen . Claes . Owen . David R. . Philip . John . Rubin . Donald B. . Stocking . Martha . August 13, 1976 . Criminality in XYY and XXY men . . 193 . 4253 . 547–555 . 10.1126/science.959813 . 1742747 . 959813. 1976Sci...193..547W .
- News: Knox, Richard . August 11, 1976 . Males with extra chromosomes not violence-prone, Danish study shows . . 5 . July 7, 2017 . January 31, 2013 . https://archive.today/20130131200106/http://pqasb.pqarchiver.com/boston/access/1976214812.html?FMT=ABS&FMTS=ABS:AI . dead .
- August 14, 1976 . XYY: No link to aggressive crime . . 110 . 7 . 103 . 3961261.
- August 30, 1976 . Medicine: Capsules . . 108 . 9 . 58 . February 8, 2012 . August 14, 2013 . https://web.archive.org/web/20130814015954/http://www.time.com/time/magazine/article/0,9171,918265,00.html . dead .
- News: Brody, Jane E. . September 12, 1976 . A chromosome link to crime is doubted; Study in Denmark finds no data to back view that 'XYY' men are inclined to be violent . . 18 .
- The five March of Dimes international conferences and four books also included reports on the findings of longitudinal prospective studies in London, Ontario and Tokyo on the development of children and with sex chromosome abnormalities identified in part by newborn screening programs.
- The last active longitudinal prospective study ended in 2000 with the end of the 36-year Denver study following the death of pediatrician and geneticist Arthur Robinson.
- Book: Robinson, Arthur . Linden, Mary G. . Bender, Bruce G. . 1998 . Prenatal diagnosis of sex chromosome abnormalities . 249–285 . Milunsky, Aubrey . Genetic disorders and the fetus : diagnosis, prevention and treatment . 4th . Baltimore . . 978-0-8018-5801-7.
- May–June 2001 . Life adaptation in 35 adults with sex chromosome abnormalities . . 3 . 3 . 187–191 . 11388759 . Bender, Bruce G. . Linden, Mary G. . Harmon, Robert J. . 10.1097/00125817-200105000-00007. free .
- Rao . Ercole . Weiss . Birgit . Fukami . Maki . Rump . Andreas . Niesler . Beate . Mertz . Annelyse . Muroya . Koji . Binder . Gerhard . Kirsch . Stefan . Winkelmann . Martina . Nordsiek . Gabriele . Heinrich . Udo . Breuning . Martijn H. . Ranke . Michael B. . Rosenthal . André . Ogata . Tsutomu . Rappold . Gudrun A. . May 1997 . Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome . . 16 . 1 . 54–63 . 10.1038/ng0597-54 . 9140395. 26248561 .
- Götz . Michael J. . Johnstone . Eve C. . Ratcliffe . Shirley G. . July 1999 . Criminality and antisocial behaviour in unselected men with sex chromosome abnormalities . . 29 . 4 . 953–962 . 10.1017/S0033291799008594 . 10473322. 23208917 .
- Robinson, Arthur . April 1990 . Living history: an autobiography of Arthur Robinson . . 35 . 4 . 475–480 . 10.1002/ajmg.1320350406 . 2185631.
- Linden, Mary G. . Bender, Bruce G. . June 1, 2002 . Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities . . 110 . 1 . 11–18 . 12116265 . 10.1002/ajmg.10394.
- Book: Gravholt, Claus Højbjerg . 2013 . Sex chromosome abnormalities . Pyeritz . Reed E. . Rimoin . David L. . Korf . Bruce R. . Emery and Rimoin's principles and practice of medical genetics . 6th . 1180–1211 . San Diego . . 978-0-12-383834-6 . This sex chromosome aneuploidy is not characterized by distinct physical features and, because there does not appear to be recognizable pattern of neurodevelopment or behavioral characteristics, the use of the term syndrome may be inappropriate. Males with an extra Y chromosome are phenotypically normal and most never come to medical attention.
Pubertal development, testicular histology, and spermatogenesis are most often normal.
…it appears that XY pairing and recombination occur normally in 47,XYY, the extra Y chromosome being lost during spermatogenesis, so that many XYY men have fathered chromosomally normal children. It has generally been observed that reproductive risks for males with 47,XYY are no higher than for euploid males, despite the fact that in situ hybridization studies demonstrated a lower frequency of single Y-bearing sperm than expected and a variably higher rate of disomic XX, XY and YY spermatozoa in males with 47,XYY.
Population-based studies have demonstrated that intellectual abilities tend to be slightly lower than those of siblings and matched controls and that boys with an extra Y chromosome are more likely to require educational help. However, intelligence is usually well within the normal range.
During school age, learning disabilities requiring educational intervention are present in approximately 50% and are as responsive to therapy as they are in children with normal chromosomes. Expressive and receptive language delays and reading disorders are common..
- Book: Milunsky, Jeff M. . 2010 . Prenatal diagnosis of sex chromosome abnormalities . 273–312 . Milunsky, Aubrey . Milunsky, Jeff M. . Genetic disorders and the fetus: diagnosis, prevention and treatment . 6th . Oxford . . 978-1-4051-9087-9. The addition of a Y chromosome to a normal male chromosome constitution does not produce a discernible phenotype. Males with 47,XYY cannot be characterized by discriminating physical or behavioral features. The first diagnosis of this condition, therefore, was a karyotypic and not a phenotypic discovery.
Pubertal development is normal and these men are usually fertile..
- Book: Royce, Kenneth . June 1, 1970 . The XYY Man . London . . 978-0-340-10694-5.
- News: Kneeland, Harold . December 8, 1970 . Books: Antiheroes and villains . . B6 . The genetic fable is The XYY Man by Kenneth Royce (David McKay, $4.95). It leans so lightly on the theory that an extra Y chromosome produces a criminal that the reader can forget the biology and enjoy the fast footwork. Royce has simply manufactured a super cat burglar who is euchered into working for MI6. This tall (that chromosome), intelligent (that chromosome again), functionally nonviolent (that chromosome still again) fellow plays the damndest game with British internal security that ever filled a dossier... . July 7, 2017 . October 26, 2012 . https://web.archive.org/web/20121026103543/http://pqasb.pqarchiver.com/washingtonpost_historical/access/158533992.html?FMT=ABS&FMTS=ABS:AI . dead .
- Book: Fulton, Roger . Betancourt, John . 1998 . Doomwatch . The Sci-Fi Channel encyclopedia of TV science fiction . New York . . 978-0-446-67478-2. 170. By the Pricking of My Thumbs ... written by Robin Chapman. Sixteen-year-old Stephen Franklin is expelled from school because, his father says, he has an obscure genetic defect—an extra "Y" chromosome.
- News: Roush, Matt . November 17, 1993 . Critic's corner . . 12D . July 7, 2017 . October 26, 2012 . https://web.archive.org/web/20121026113939/http://pqasb.pqarchiver.com/USAToday/access/55220486.html?FMT=ABS&FMTS=ABS:FT . dead . One of TV's most consistently rewarding series takes a grim and unforgettable detour into the bleak mindset of a teen-age sociopathic murderer. Is society to blame, or as his lawyer argues, is he genetically predisposed to violence, with an extra "Y" chromosome? … the boy's hopeless future seems all too evident.
- Hochman, David . May 7–13, 2007 . Horatio hunts a natural-born killer . . 55 . 19 . 34–36. There's nothing funny about the season finale. That episode is about a serial killer with "criminal" genes. "It's a real-life natural-born killer situation", executive producer Ann Donahue says. "Usually girls have XX chromosomes and boys have XY, but this killer is XYY, which means too much testosterone." Among other niceties, the killer who has ties to Boston… brands his female victims with the letter Y.
- dir. Van Fischer . 2005 . . film. en . 10m00s.