396 related articles for article (PubMed ID: 11426451)
1. Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients.
Iitsuka Y; Bock A; Nguyen DD; Samango-Sprouse CA; Simpson JL; Bischoff FZ
Am J Med Genet; 2001 Jan; 98(1):25-31. PubMed ID: 11426451
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant.
Höckner M; Pinggera GM; Günther B; Sergi C; Fauth C; Erdel M; Kotzot D
Fertil Steril; 2008 Nov; 90(5):2009.e13-7. PubMed ID: 18687426
[TBL] [Abstract][Full Text] [Related]
4. The influence of parental origin of X chromosome genes on the stature of patients with 45 X Turner syndrome.
Kochi C; Longui CA; Lemos-Marini SH; Guerra-Junior G; Melo MB; Calliari LE; Monte O
Genet Mol Res; 2007 Jan; 6(1):1-7. PubMed ID: 17278084
[TBL] [Abstract][Full Text] [Related]
5. Chromosomal variants in klinefelter syndrome.
Frühmesser A; Kotzot D
Sex Dev; 2011; 5(3):109-23. PubMed ID: 21540567
[TBL] [Abstract][Full Text] [Related]
6. The parental origin of 47,XXY males.
Harvey J; Jacobs PA; Hassold T; Pettay D
Birth Defects Orig Artic Ser; 1990; 26(4):289-96. PubMed ID: 2090327
[TBL] [Abstract][Full Text] [Related]
7. Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.
Zaki MS; Kamel AA; El-Ruby M
Genet Couns; 2005; 16(4):393-402. PubMed ID: 16440882
[TBL] [Abstract][Full Text] [Related]
8. A simple screening method for detection of Klinefelter syndrome and other X-chromosome aneuploidies based on copy number of the androgen receptor gene.
Ottesen AM; Garn ID; Aksglaede L; Juul A; Rajpert-De Meyts E
Mol Hum Reprod; 2007 Oct; 13(10):745-50. PubMed ID: 17720778
[TBL] [Abstract][Full Text] [Related]
9. Germ cell development in the XXY mouse: evidence that X chromosome reactivation is independent of sexual differentiation.
Mroz K; Carrel L; Hunt PA
Dev Biol; 1999 Mar; 207(1):229-38. PubMed ID: 10049577
[TBL] [Abstract][Full Text] [Related]
10. Rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome: case report.
Velissariou V; Christopoulou S; Karadimas C; Pihos I; Kanaka-Gantenbein C; Kapranos N; Kallipolitis G; Hatzaki A
Eur J Med Genet; 2006; 49(4):331-7. PubMed ID: 16829354
[TBL] [Abstract][Full Text] [Related]
11. Novel genetic aspects of Klinefelter's syndrome.
Tüttelmann F; Gromoll J
Mol Hum Reprod; 2010 Jun; 16(6):386-95. PubMed ID: 20228051
[TBL] [Abstract][Full Text] [Related]
12. Male-to-male transmission of X-linked Alport syndrome in a boy with a 47,XXY karyotype.
Ars E; Tazón-Vega B; Ruiz P; Nogués C; Arnedo N; Rajmil O; Torra R
Eur J Hum Genet; 2005 Sep; 13(9):1040-6. PubMed ID: 15957001
[TBL] [Abstract][Full Text] [Related]
13. Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1.
Lose F; Duffy DL; Kay GF; Kedda MA; Spurdle AB; ;
J Natl Cancer Inst; 2008 Nov; 100(21):1519-29. PubMed ID: 18957670
[TBL] [Abstract][Full Text] [Related]
14. Genotype and phenotype in Klinefelter syndrome - impact of androgen receptor polymorphism and skewed X inactivation.
Bojesen A; Hertz JM; Gravholt CH
Int J Androl; 2011 Dec; 34(6 Pt 2):e642-8. PubMed ID: 21977989
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Methylation-specific PCR allows for fast diagnosis of X chromosome disomy and reveals skewed inactivation of the X chromosome in men with Klinefelter syndrome.
Mehta A; Malek-Jones M; Bolyakov A; Mielnik A; Schlegel PN; Paduch DA
J Androl; 2012; 33(5):955-62. PubMed ID: 22441764
[TBL] [Abstract][Full Text] [Related]
17. Mental development in polysomy X Klinefelter syndrome (47,XXY; 48,XXXY): effects of incomplete X inactivation.
Samango-Sprouse C
Semin Reprod Med; 2001 Jun; 19(2):193-202. PubMed ID: 11480917
[TBL] [Abstract][Full Text] [Related]
18. Neuropsychology and brain morphology in Klinefelter syndrome - the impact of genetics.
Skakkebaek A; Bojesen A; Kristensen MK; Cohen A; Hougaard DM; Hertz JM; Fedder J; Laurberg P; Wallentin M; Østergaard JR; Pedersen AD; Gravholt CH
Andrology; 2014 Jul; 2(4):632-40. PubMed ID: 24865607
[TBL] [Abstract][Full Text] [Related]
19. Transmission-ratio distortion of X chromosomes among male offspring of females with skewed X-inactivation.
Naumova AK; Olien L; Bird LM; Slamka C; Fonseca M; Verner AE; Wang M; Leppert M; Morgan K; Sapienza C
Dev Genet; 1995; 17(3):198-205. PubMed ID: 8565326
[TBL] [Abstract][Full Text] [Related]
20. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
