Results 31 to 40 of about 7,045,534 (115)

Radioulnar synostosis and XYY syndrome.

, 2000
A case report of a child with XYY syndrome and radioulnar ...
Guala A, Licata D, Franceschini P, Franceschini D., DI CARA, GIUSEPPE   +4 more
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XYY: Why? Science for the People and the XYY Controversy [PDF]

The mid-20th century saw a boom of scientific discoveries in genetics as people sought to understand the American political landscape through genomes. The desire to understand criminality through genetics rose as counterculture surged. The genetic defect
Rice, Fern
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NF1 with 47,XYY mosaicism diagnosed by mandibular neurofibromas

Neurofibromatosis type 1 (NF1) is an autosomal dominant nevus disease characterized by multiple manifestations, primarily café-au-lait macules and neurofibromas.
Kyoko Hoshino, Kei-ichi Morita, Yosuke Harazono, Erina Tonouchi, Tetsuya Yoda   +4 more
core   +1 more source

Characterization of autism spectrum disorder and neurodevelopmental profiles in youth with XYY syndrome

, 2018
Background XYY syndrome is a sex chromosome aneuploidy that occurs in ~ 1/850 male births and is associated with increased risk for neurodevelopmental difficulties.
Cristan Farmer, Ari Fish, Laura Henry, Jonathan Blumenthal, Jakob Seidlitz, Armin Raznahan, Anastasia Xenophontos, Erin Torres, Audrey Thurm, Colby Chlebowski, Liv Clasen, Lisa Joseph, Catherine Mankiw, Bethany Sauls   +13 more
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Pregnancy outcomes in prenatally diagnosed 47,XXX and 47,XYY syndromes: a 30-year French, retrospective, multicentre study

, 2016
International audienceOBJECTIVE: Sex chromosome aneuploidies are frequently detected fortuitously in a prenatal diagnosis. Most cases of 47,XXX and 47,XYY syndromes are diagnosed in this context, and parents are thus faced with an unexpected situation ...
Vialard, François, Jimenez, Mélanie, Amblard, Florence, Mugneret, Francine, Flori, Elisabeth, Collonge-Rame, Marie-Agnès, Carré-Pigeon, Frédérique, Lebel-Roy, Camille, Harbuz, Radu, Le Meur, Nathalie, Till, Marianne, Yardin, Catherine, Gruchy, Nicolas, Herbaux, Martine, Vigouroux-Castera, Adeline, Jaillard, Sylvie, Vago, Philippe, Valduga, Mylène, Leporrier, Nathalie, Chambon, Pascal, Coussement, Aurélie, Joly-Helas, Géraldine, Blondeel, Eléonore, Lespinasse, James   +23 more
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Study on Absorption, Distribution and Excretion of a New Candidate Compound XYY-CP1106 against Alzheimer’s Disease in Rats by LC-MS/MS

, 2023
XYY-CP1106, a candidate compound synthesized from a hybrid of hydroxypyridinone and coumarin, has been shown to be remarkably effective in treating Alzheimer’s disease.
Zili Guo, Bianbian Gao, Weike Su, Lisha Chen, Yuanyuan Xie, Miaoliang Fan, Xianrui Liang, Changjun Zhang   +7 more
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A Case of Full Term Delivery of a Child with 47 , XYY Subsequent to Prenatal Diagnosis at Midtrimester [PDF]

, 2001
47,XYY is a rare sex chromosomal disorder. Approximately 1.45 per 1,000 live births have on XYY chromosome pattern. The extra Y chromosome is paternal in origin and results from nondisjunction in the second meiotic division.
김세광
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Diagnosis and mortality in 47,XYY persons: a registry study [PDF]

, 2010
Background Sex chromosomal abnormalities are relatively common, yet many aspects of these syndromes remain unexplored. For instance epidemiological data in 47,XYY persons are still limited.
Stochholm Kirstine, Svend Juul, Claus H Gravholt, Juul Svend, Gravholt Claus H, Kirstine Stochholm   +5 more
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Double Aneuploidy of Down Syndrome (Trisomy 21) and Jacobs Syndrome (Trisomy XYY) with Complete Tracheal Rings Deformity: Case Report and Literature Review

, 2023
Down syndrome (DS, trisomy 21) with an extra copy of chromosome 21 is one of the most common aneuploidies in humans. Jacobs syndrome or XYY syndrome (trisomy XYY) with an extra copy of sex chromosome Y is a rare sex chromosome trisomy in males.
Bhuvaneshwari Jagadesan, Omoloro Adeleke, Hussein Elmufti, Jie Zhang, Mimily Harsono   +4 more
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Criminality in men with Klinefelter's syndrome and XYY syndrome:a cohort study

, 2012
To investigate the criminal pattern in men between 15 and 70 years of age diagnosed with 47,XXY (Klinefelter's syndrome (KS)) or 47,XYY compared to the general ...
Jensen, Anne Skakkebæk, Stochholm, Kirstine, Bojesen, Anders, Juul, Svend, Gravholt, Claus Højbjerg   +4 more
core   +1 more source