252 related articles for article (PubMed ID: 20014371)
21. The Klinefelter syndrome is associated with high recurrence of copy number variations on the X chromosome with a potential role in the clinical phenotype.
Rocca MS; Pecile V; Cleva L; Speltra E; Selice R; Di Mambro A; Foresta C; Ferlin A
Andrology; 2016 Mar; 4(2):328-34. PubMed ID: 26789125
[TBL] [Abstract][Full Text] [Related]
22. Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome.
Zinn AR; Ramos P; Elder FF; Kowal K; Samango-Sprouse C; Ross JL
J Clin Endocrinol Metab; 2005 Sep; 90(9):5041-6. PubMed ID: 15956082
[TBL] [Abstract][Full Text] [Related]
23. Klinefelter syndrome and other sex chromosomal aneuploidies.
Visootsak J; Graham JM
Orphanet J Rare Dis; 2006 Oct; 1():42. PubMed ID: 17062147
[TBL] [Abstract][Full Text] [Related]
24. Salivary testosterone in relation to social cognition and social anxiety in children and adolescents with 47,XXY (Klinefelter syndrome).
van Rijn S
PLoS One; 2018; 13(7):e0200882. PubMed ID: 30036387
[TBL] [Abstract][Full Text] [Related]
25. [Gonosomal trisomy syndrome. Five case reports and review of literature].
Schwemmle C; Jungheim M; Ptok M
Laryngorhinootologie; 2013 Nov; 92(11):725-31. PubMed ID: 23929211
[TBL] [Abstract][Full Text] [Related]
26. 49,XXXXY syndrome: A study of neurological function in this uncommon X and Y chromosomal disorder.
Samango-Sprouse C; Lasutschinkow PC; Mitchell F; Porter GF; Hendrie P; Powell S; Sadeghin T; Gropman A
Am J Med Genet A; 2021 Dec; 185(12):3557-3566. PubMed ID: 32656941
[TBL] [Abstract][Full Text] [Related]
27. Variant Klinefelter syndrome 47,X,i(X)(q10),Y and normal 46,XY karyotype in monozygotic adult twins.
Stemkens D; Broekmans FJ; Kastrop PM; Hochstenbach R; Smith BG; Giltay JC
Am J Med Genet A; 2007 Aug; 143A(16):1906-11. PubMed ID: 17632769
[TBL] [Abstract][Full Text] [Related]
28. The epidemiology of sex chromosome abnormalities.
Berglund A; Stochholm K; Gravholt CH
Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):202-215. PubMed ID: 32506765
[TBL] [Abstract][Full Text] [Related]
29. The psychoeducational profile of boys with Klinefelter syndrome.
Rovet J; Netley C; Keenan M; Bailey J; Stewart D
J Learn Disabil; 1996 Mar; 29(2):180-96. PubMed ID: 8820203
[TBL] [Abstract][Full Text] [Related]
30. [Incidence of 47,XXY and 47,XYY karyotypes among the mentally ill who have committed antisocial acts].
Marinina GP
Genetika; 1981; 17(1):165-73. PubMed ID: 7194833
[TBL] [Abstract][Full Text] [Related]
31. Dysregulation of X-linked gene expression in Klinefelter's syndrome and association with verbal cognition.
Vawter MP; Harvey PD; DeLisi LE
Am J Med Genet B Neuropsychiatr Genet; 2007 Sep; 144B(6):728-34. PubMed ID: 17347996
[TBL] [Abstract][Full Text] [Related]
32. Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndrome.
Wikström AM; Painter JN; Raivio T; Aittomäki K; Dunkel L
Clin Endocrinol (Oxf); 2006 Jul; 65(1):92-7. PubMed ID: 16817826
[TBL] [Abstract][Full Text] [Related]
33. Neuropsychological profiles of adults with Klinefelter syndrome.
Boone KB; Swerdloff RS; Miller BL; Geschwind DH; Razani J; Lee A; Gonzalo IG; Haddal A; Rankin K; Lu P; Paul L
J Int Neuropsychol Soc; 2001 May; 7(4):446-56. PubMed ID: 11396547
[TBL] [Abstract][Full Text] [Related]
34. Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome.
Gropman AL; Rogol A; Fennoy I; Sadeghin T; Sinn S; Jameson R; Mitchell F; Clabaugh J; Lutz-Armstrong M; Samango-Sprouse CA
Am J Med Genet A; 2010 Jun; 152A(6):1523-30. PubMed ID: 20503329
[TBL] [Abstract][Full Text] [Related]
35. Cognition, Academic Achievement, Adaptive Behavior, and Quality of Life in Child and Adolescent Boys with Klinefelter Syndrome.
Jordan TL; Foland-Ross LC; Wun VL; Ross JL; Reiss AL
J Dev Behav Pediatr; 2023 Sep; 44(7):e476-e485. PubMed ID: 37696031
[TBL] [Abstract][Full Text] [Related]
36. The contribution of Xp22.31 gene dosage to Turner and Klinefelter syndromes and sex-biased phenotypes.
Davies W
Eur J Med Genet; 2021 Apr; 64(4):104169. PubMed ID: 33610733
[TBL] [Abstract][Full Text] [Related]
37. Detection and characterization of male sex chromosome abnormalities in the UK Biobank study.
Zhao Y; Gardner EJ; Tuke MA; Zhang H; Pietzner M; Koprulu M; Jia RY; Ruth KS; Wood AR; Beaumont RN; Tyrrell J; Jones SE; Lango Allen H; Day FR; Langenberg C; Frayling TM; Weedon MN; Perry JRB; Ong KK; Murray A
Genet Med; 2022 Sep; 24(9):1909-1919. PubMed ID: 35687092
[TBL] [Abstract][Full Text] [Related]
38. Incidence of Y chromosome microdeletions in patients with Klinefelter syndrome.
Sciarra F; Pelloni M; Faja F; Pallotti F; Martino G; Radicioni AF; Lenzi A; Lombardo F; Paoli D
J Endocrinol Invest; 2019 Jul; 42(7):833-842. PubMed ID: 30499012
[TBL] [Abstract][Full Text] [Related]
39. International investigation of neurocognitive and behavioral phenotype in 47,XXY (Klinefelter syndrome): Predicting individual differences.
Samango-Sprouse C; Stapleton E; Chea S; Lawson P; Sadeghin T; Cappello C; de Sonneville L; van Rijn S
Am J Med Genet A; 2018 Apr; 176(4):877-885. PubMed ID: 29423966
[TBL] [Abstract][Full Text] [Related]
40. Klinefelter syndrome comorbidities linked to increased X chromosome gene dosage and altered protein interactome activity.
Belling K; Russo F; Jensen AB; Dalgaard MD; Westergaard D; Rajpert-De Meyts E; Skakkebæk NE; Juul A; Brunak S
Hum Mol Genet; 2017 Apr; 26(7):1219-1229. PubMed ID: 28369266
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
