366 related articles for article (PubMed ID: 9890065)
1. Abnormalities of gonadal differentiation.
Berkovitz GD; Seeherunvong T
Baillieres Clin Endocrinol Metab; 1998 Apr; 12(1):133-42. PubMed ID: 9890065
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Candidate genes in complete and partial XY sex reversal: mutation analysis of SRY, SRY-related genes and FTZ-F1.
Lim HN; Freestone SH; Romero D; Kwok C; Hughes IA; Hawkins JR
Mol Cell Endocrinol; 1998 May; 140(1-2):51-8. PubMed ID: 9722168
[TBL] [Abstract][Full Text] [Related]
5. Is true hermaphroditism a primary germ cell disorder?
McKelvie P; Jaubert F; Nezelof C
Pediatr Pathol; 1987; 7(1):31-41. PubMed ID: 3601818
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. The role of SRY in mammalian sex determination.
Fechner PY
Acta Paediatr Jpn; 1996 Aug; 38(4):380-9. PubMed ID: 8840551
[TBL] [Abstract][Full Text] [Related]
8. Absence of the testicular determining factor gene SRY in XX true hermaphrodites and presence of this locus in most subjects with gonadal dysgenesis caused by Y aneuploidy.
Tho SP; Layman LC; Lanclos KD; Plouffe L; Byrd JR; McDonough PG
Am J Obstet Gynecol; 1992 Dec; 167(6):1794-802. PubMed ID: 1471700
[TBL] [Abstract][Full Text] [Related]
9. Molecular analysis of SRY gene in Brazilian 46,XX sex reversed patients: absence of SRY sequence in gonadal tissue.
Domenice S; Nishi MY; Billerbeck AE; Carvalho FM; Frade EM; Latronico AC; Arnhold IJ; Mendonca BB
Med Sci Monit; 2001; 7(2):238-41. PubMed ID: 11257728
[TBL] [Abstract][Full Text] [Related]
10. [Causes of ambiguous external genitalia in neonates].
Zdravković D; Milenković T; Sedlecki K; Guć-Sćekić M; Rajić V; Banićević M
Srp Arh Celok Lek; 2001; 129(3-4):57-60. PubMed ID: 11534268
[TBL] [Abstract][Full Text] [Related]
11. Molecular analysis in true hermaphrodites with different karyotypes and similar phenotypes.
Torres L; López M; Méndez JP; Canto P; Cervantes A; Alfaro G; Pérez-Palacios G; Erickson RP; Kofman-Alfaro S
Am J Med Genet; 1996 May; 63(2):348-55. PubMed ID: 8725784
[TBL] [Abstract][Full Text] [Related]
12. Monozygotic twins of opposite sex.
Wachtel SS; Somkuti SG; Schinfeld JS
Cytogenet Cell Genet; 2000; 91(1-4):293-5. PubMed ID: 11173871
[TBL] [Abstract][Full Text] [Related]
13. Mutation analysis of subjects with 46, XX sex reversal and 46, XY gonadal dysgenesis does not support the involvement of SOX3 in testis determination.
Lim HN; Berkovitz GD; Hughes IA; Hawkins JR
Hum Genet; 2000 Dec; 107(6):650-2. PubMed ID: 11153920
[TBL] [Abstract][Full Text] [Related]
14. Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesis.
Pivnick EK; Wachtel S; Woods D; Simpson JL; Bishop CE
Hum Genet; 1992 Nov; 90(3):308-10. PubMed ID: 1487248
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Molecular analysis in true hermaphroditism: demonstration of low-level hidden mosaicism for Y-derived sequences in 46,XX cases.
Queipo G; Zenteno JC; Peña R; Nieto K; Radillo A; Dorantes LM; Eraña L; Lieberman E; Söderlund D; Jiménez AL; Ramón G; Kofman-Alfaro S
Hum Genet; 2002 Sep; 111(3):278-83. PubMed ID: 12215841
[TBL] [Abstract][Full Text] [Related]
17. XX Maleness and XX true hermaphroditism in SRY-negative monozygotic twins: additional evidence for a common origin.
Maciel-Guerra AT; de Mello MP; Coeli FB; Ribeiro ML; Miranda ML; Marques-de-Faria AP; Baptista MT; Moraes SG; Guerra-Júnior G
J Clin Endocrinol Metab; 2008 Feb; 93(2):339-43. PubMed ID: 18056774
[TBL] [Abstract][Full Text] [Related]
18. A rare case of 46,XX true hermaphroditism with hidden mosaicism with sex-determining region Y chromosome-bearing cells in the gonads.
Inoue H; Nomura M; Yanase T; Ichino I; Goto K; Ikuyama S; Takayanagi R; Nawata H
Intern Med; 1998 May; 37(5):467-71. PubMed ID: 9652903
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Combined Leydig cell and Sertoli cell dysfunction in 46,XX males lacking the sex determining region Y gene.
Turner B; Fechner PY; Fuqua JS; Marcantonio SM; Perlman EJ; Vordermark JS; Berkovitz GD
Am J Med Genet; 1995 Jul; 57(3):440-3. PubMed ID: 7677147
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]