100 related articles for article (PubMed ID: 9450909)
1. 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]
2. 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]
3. Mutational analysis of SRY in XY females.
Hawkins JR
Hum Mutat; 1993; 2(5):347-50. PubMed ID: 8257986
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Complete XY gonadal dysgenesis and aspects of the SRYgenotype and gonadal tumor formation.
Uehara S; Hashiyada M; Sato K; Nata M; Funato T; Okamura K
J Hum Genet; 2002; 47(6):279-84. PubMed ID: 12111377
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Structural basis for SRY-dependent 46-X,Y sex reversal: modulation of DNA bending by a naturally occurring point mutation.
Murphy EC; Zhurkin VB; Louis JM; Cornilescu G; Clore GM
J Mol Biol; 2001 Sep; 312(3):481-99. PubMed ID: 11563911
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. Identification of a novel mutation in the SRY gene in a 46, XY female patient.
Salehi LB; Scarciolla O; Vanni GF; Nardone AM; Frajese G; Novelli G; Stuppia L
Eur J Med Genet; 2006; 49(6):494-8. PubMed ID: 16675314
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Analysis of the SRY gene in two sex-reversed XY sisters identifies two new novel point mutations in the high mobility group box domain.
Shahid M; Dhillon VS; Hussain Z; Masa JF; Aslam M; Raish M; Ahmad A; Khan NJ; Prasad S; Batra S; Pasha ST; Husain SA
Fertil Steril; 2008 Oct; 90(4):1199.e1-8. PubMed ID: 18304538
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Biochemical defects in eight SRY missense mutations causing XY gonadal dysgenesis.
Mitchell CL; Harley VR
Mol Genet Metab; 2002 Nov; 77(3):217-25. PubMed ID: 12409269
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. The molecular genetic jigsaw puzzle of vertebrate sex determination and its missing pieces.
Scherer G
Novartis Found Symp; 2002; 244():225-36; discussion 236-9, 253-7. PubMed ID: 11990793
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
