110 related articles for article (PubMed ID: 10203670)
1. Prenatal diagnosis of 46,XX male fetuses.
Ginsberg NA; Cadkin A; Strom C; Bauer-Marsh E; Verlinsky Y
Am J Obstet Gynecol; 1999 Apr; 180(4):1006-7. PubMed ID: 10203670
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of a 45,X male with a SRY-bearing chromosome 21.
Nataf V; Senat MV; Albert M; Bidat L; de Mazancourt P; Roume J; Allard L; Le Tessier D; Ville Y; Selva J
Prenat Diagn; 2002 Aug; 22(8):675-80. PubMed ID: 12210575
[TBL] [Abstract][Full Text] [Related]
3. SRY-negative XX fetus with complete male phenotype.
Vilain E; Le Fiblec B; Morichon-Delvallez N; Brauner R; Dommergues M; Dumez Y; Jaubert F; Boucekkine C; McElreavey K; Vekemans M
Lancet; 1994 Jan; 343(8891):240-1. PubMed ID: 7904700
[No Abstract] [Full Text] [Related]
4. Analysis of the testis-determining gene SRY in patients with XY gonadal dysgenesis.
Tsutsumi O; Iida T; Nakahori Y; Taketani Y
Horm Res; 1996; 46 Suppl 1():6-10. PubMed ID: 8864741
[TBL] [Abstract][Full Text] [Related]
5. Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination.
McElreavey K; Vilain E; Barbaux S; Fuqua JS; Fechner PY; Souleyreau N; Doco-Fenzy M; Gabriel R; Quereux C; Fellous M; Berkovitz GD
Proc Natl Acad Sci U S A; 1996 Aug; 93(16):8590-4. PubMed ID: 8710915
[TBL] [Abstract][Full Text] [Related]
6. Identification of a new missense mutation (Gly95Glu) in a highly conserved codon within the high-mobility group box of the sex-determining region Y gene: report on a 46,XY female with gonadal dysgenesis and yolk-sac tumor.
Schäffler A; Barth N; Winkler K; Zietz B; Rümmele P; Knüchel R; Schölmerich J; Palitzsch KD
J Clin Endocrinol Metab; 2000 Jun; 85(6):2287-92. PubMed ID: 10852465
[TBL] [Abstract][Full Text] [Related]
7. Molecular cytogenetic analysis of XX males using Y-specific DNA sequences, including SRY.
Van der Auwera B; Van Roy N; De Paepe A; Hawkins JR; Liebaers I; Castedo S; Dumon J; Speleman F
Hum Genet; 1992 Apr; 89(1):23-8. PubMed ID: 1577463
[TBL] [Abstract][Full Text] [Related]
8. Testis determining gene(s) on the X chromosome short arm: chromosomal localisation and possible role in testis determination.
Ogata T; Matsuo N
J Med Genet; 1994 Apr; 31(4):349. PubMed ID: 8071967
[No Abstract] [Full Text] [Related]
9. Deletion of the Sry region on the Y chromosome detected in a case of equine gonadal hypoplasia (XY female) with abnormal hormonal profiles.
Abe S; Miyake YI; Kageyama SI; Watanabe G; Taya K; Kawakura K
Equine Vet J; 1999 Jul; 31(4):336-8. PubMed ID: 10454094
[No Abstract] [Full Text] [Related]
10. Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.
Margarit E; Soler A; Carrió A; Oliva R; Costa D; Vendrell T; Rosell J; Ballesta F
J Med Genet; 1998 Sep; 35(9):727-30. PubMed ID: 9733030
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of sex differentiation disorders: the role of fetal ultrasound.
Pinhas-Hamiel O; Zalel Y; Smith E; Mazkereth R; Aviram A; Lipitz S; Achiron R
J Clin Endocrinol Metab; 2002 Oct; 87(10):4547-53. PubMed ID: 12364433
[TBL] [Abstract][Full Text] [Related]
12. Two SRY-negative XX male brothers without genital ambiguity.
Zenteno JC; López M; Vera C; Méndez JP; Kofman-Alfaro S
Hum Genet; 1997 Oct; 100(5-6):606-10. PubMed ID: 9341880
[TBL] [Abstract][Full Text] [Related]
13. The role of sexual related Y gene detection in the diagnosis of patients with gonadal dysgenesis.
Yu Q; Huang S; Ye L; Feng L; He F; Ye J; Gu C; Ge Q
Chin Med J (Engl); 2001 Feb; 114(2):128-31. PubMed ID: 11780190
[TBL] [Abstract][Full Text] [Related]
14. SRY protein is expressed in ovotestis and streak gonads from human sex-reversal.
Salas-Cortés L; Jaubert F; Nihoul-Feketé C; Brauner R; Rosemblatt M; Fellous M
Cytogenet Cell Genet; 2000; 91(1-4):212-6. PubMed ID: 11173859
[TBL] [Abstract][Full Text] [Related]
15. [Sex genetics].
Vilain E; Elreavey KM; Richaud F; Fellous M
Presse Med; 1992 May; 21(18):852-6. PubMed ID: 1535151
[TBL] [Abstract][Full Text] [Related]
16. Presence of Y chromosome sequences and their effect on the phenotype of six patients with Y chromosome anomalies.
Shankman S; Spurdle AB; Morris D; Rosendorff J; Marques I; Bernstein R; Ramsay M
Am J Med Genet; 1995 Jan; 55(3):269-75. PubMed ID: 7726221
[TBL] [Abstract][Full Text] [Related]
17. An autosomal or X linked mutation results in true hermaphrodites and 46,XX males in the same family.
Slaney SF; Chalmers IJ; Affara NA; Chitty LS
J Med Genet; 1998 Jan; 35(1):17-22. PubMed ID: 9475089
[TBL] [Abstract][Full Text] [Related]
18. An SRY-negative XX male with Huriez syndrome.
Vernole P; Terrinoni A; Didona B; De Laurenzi V; Rossi P; Melino G; Grimaldi P
Clin Genet; 2000 Jan; 57(1):61-6. PubMed ID: 10733237
[TBL] [Abstract][Full Text] [Related]
19. An SRY-negative 47,XXY mother and daughter.
Röttger S; Schiebel K; Senger G; Ebner S; Schempp W; Scherer G
Cytogenet Cell Genet; 2000; 91(1-4):204-7. PubMed ID: 11173857
[TBL] [Abstract][Full Text] [Related]
20. Absence of Turner stigmata in a 46,XYp-female.
Müller U; Kirkels VG; Scheres JM
Hum Genet; 1992 Nov; 90(3):239-42. PubMed ID: 1487236
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]