101 related articles for article (PubMed ID: 12568875)
1. In syndromes of confused gonads, height can be important!
McDonough PG
Fertil Steril; 2003 Feb; 79(2):462-3. PubMed ID: 12568875
[No Abstract] [Full Text] [Related]
2. In syndromes of confused gonads, height can be important!
Edmonds DK
Fertil Steril; 2003 Feb; 79(2):461; author reply 461. PubMed ID: 12568873
[No Abstract] [Full Text] [Related]
3. Novel mutation in the SRY gene results in 46,XY gonadal dysgenesis.
Cameron FJ; Smith MJ; Warne GL; Sinclair AH
Hum Mutat; 1998; Suppl 1():S110-1. PubMed ID: 9452057
[No Abstract] [Full Text] [Related]
4. Mutation in the 5' noncoding region of the SRY gene in an XY sex-reversed patient.
Poulat F; Desclozeaux M; Tuffery S; Jay P; Boizet B; Berta P
Hum Mutat; 1998; Suppl 1():S192-4. PubMed ID: 9452083
[No Abstract] [Full Text] [Related]
5. Analysis of the SRY gene in gonadal tissue of subjects with 46,XY gonadal dysgenesis.
Fuqua JS; McLaughlin J; Perlman EJ; Berkovitz GD
J Clin Endocrinol Metab; 1997 Feb; 82(2):701-2. PubMed ID: 9024280
[No Abstract] [Full Text] [Related]
6. Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndrome.
Veitia RA; Nunes M; Quintana-Murci L; Rappaport R; Thibaud E; Jaubert F; Fellous M; McElreavey K; Gonçalves J; Silva M; Rodrigues JC; Caspurro M; Boieiro F; Marques R; Lavinha J
Am J Hum Genet; 1998 Sep; 63(3):901-5. PubMed ID: 9718353
[No Abstract] [Full Text] [Related]
7. Independent observation of SRY mutation I90M in a patient with complete gonadal dysgenesis.
Dörk T; Stuhrmann M; Miller K; Schmidtke J
Hum Mutat; 1998; 11(1):90-1. PubMed ID: 9450909
[No Abstract] [Full Text] [Related]
8. [Molecular studies of chromosome Y in 20 patients with 46,XY karyotype].
Ben Jemaa Khemakhem L; Hila L; Mrad R; Maazoul F; Chaabouni H
Tunis Med; 1997 Oct; 75(10):762-7. PubMed ID: 9507345
[No Abstract] [Full Text] [Related]
9. A novel mutation localized in the 3' non-HMG box region of the SRY gene in 46,XY gonadal dysgenesis.
Tajima T; Nakae J; Shinohara N; Fujieda K
Hum Mol Genet; 1994 Jul; 3(7):1187-9. PubMed ID: 7981695
[No Abstract] [Full Text] [Related]
10. Detection of SRY in a 46,XY female (Swyer's syndrome).
Imai A; Horibe S; Fuseya T; Takagi H; Tamaya T
J Med; 1997; 28(1-2):49-54. PubMed ID: 9249610
[TBL] [Abstract][Full Text] [Related]
11. Ascertainment and mutational studies of SRY in nine XY females.
Graves PE; Davis D; Erickson RP; Lopez M; Kofman-Alfaro S; Mendez JP; Speer IE
Am J Med Genet; 1999 Mar; 83(2):138-9. PubMed ID: 10190485
[No Abstract] [Full Text] [Related]
12. Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations.
Scherer G; Held M; Erdel M; Meschede D; Horst J; Lesniewicz R; Midro AT
Cytogenet Cell Genet; 1998; 80(1-4):188-92. PubMed ID: 9678356
[TBL] [Abstract][Full Text] [Related]
13. Cell biology. In sex reversal, protein deterred by nuclear barrier.
Sreenivasan A
Science; 2003 Dec; 302(5653):2050. PubMed ID: 14684795
[No Abstract] [Full Text] [Related]
14. Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjects.
Kwok C; Tyler-Smith C; Mendonca BB; Hughes I; Berkovitz GD; Goodfellow PN; Hawkins JR
J Med Genet; 1996 Jun; 33(6):465-8. PubMed ID: 8782045
[TBL] [Abstract][Full Text] [Related]
15. Genetic mechanisms that regulate testis determination.
Carrillo AA; Berkovitz GD
Rev Endocr Metab Disord; 2004 Mar; 5(1):77-82. PubMed ID: 14966391
[No Abstract] [Full Text] [Related]
16. Comparison of adult height between patients with XX and XY gonadal dysgenesis: support for a Y specific growth gene(s).
Ogata T; Matsuo N
J Med Genet; 1992 Aug; 29(8):539-41. PubMed ID: 1518022
[TBL] [Abstract][Full Text] [Related]
17. Mutational analysis of SRY in XY females.
Hawkins JR
Hum Mutat; 1993; 2(5):347-50. PubMed ID: 8257986
[TBL] [Abstract][Full Text] [Related]
18. Mutations in SRY and WT1 genes required for gonadal development are not responsible for XY partial gonadal dysgenesis.
Tagliarini EB; Assumpção JG; Scolfaro MR; Mello MP; Maciel-Guerra AT; Guerra Júnior G; Hackel C
Braz J Med Biol Res; 2005 Jan; 38(1):17-25. PubMed ID: 15665984
[TBL] [Abstract][Full Text] [Related]
19. Implications of FISH investigations in MIDAS syndrome associated with a 46,XX,t(X;Y) karyotype.
Kotzot D; Hoffmann K; Kujat A; Holland H; Froster UG; Mücke J
Am J Med Genet; 2002 Nov; 113(1):108-10. PubMed ID: 12400076
[No Abstract] [Full Text] [Related]
20. 46,XY sex-reversal (Swyer syndrome) and congenital diaphragmatic hernia.
Kent A; Simpson E; Ellwood D; Silink M
Am J Med Genet A; 2004 Nov; 131(1):103-5. PubMed ID: 15389702
[No Abstract] [Full Text] [Related]
[Next] [New Search]