194 related articles for article (PubMed ID: 26817010)
1. Mixed gonadal dysgenesis in 45,X Turner syndrome with SRY gene.
Jung JY; Yang S; Jeong EH; Lee HC; Lee YM; Han HS; Yi KH
Ann Pediatr Endocrinol Metab; 2015 Dec; 20(4):226-9. PubMed ID: 26817010
[TBL] [Abstract][Full Text] [Related]
2. Gonadal dysgenesis in Turner syndrome with Y-chromosome mosaicism: Two case reports.
Leng XF; Lei K; Li Y; Tian F; Yao Q; Zheng QM; Chen ZH
World J Clin Cases; 2020 Nov; 8(22):5737-5743. PubMed ID: 33344568
[TBL] [Abstract][Full Text] [Related]
3. The role of SRY mutations in the etiology of gonadal dysgenesis in patients with 45,X/46,XY disorder of sex development and variants.
Nishi MY; Costa EM; Oliveira SB; Mendonca BB; Domenice S
Horm Res Paediatr; 2011; 75(1):26-31. PubMed ID: 20699606
[TBL] [Abstract][Full Text] [Related]
4. Description of diagnosis of 45,X/46,XY ovotesticular DSD.
Ren Š; Harmaš V; Stará M; Laštůvkováj ; Čejnová V
Ceska Gynekol; 2020; 85(4):259-262. PubMed ID: 33562981
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Partial gonadal dysgenesis in a patient with a marker Y chromosome.
Fechner PY; Smith KD; Jabs EW; Migeon CJ; Berkovitz GD
Am J Med Genet; 1992 Apr; 42(6):807-12. PubMed ID: 1313209
[TBL] [Abstract][Full Text] [Related]
7. [Pure 46,XY gonadal dysgenesis].
Ságodi L; Ladányi E; Kiss Á; Tar A; Lukács V; Minik K; Vámosi I
Orv Hetil; 2010 Nov; 151(48):1991-5. PubMed ID: 21084251
[TBL] [Abstract][Full Text] [Related]
8. Pure gonadal dysgenesis (Swyer syndrome) due to microdeletion in the SRY gene: a case report.
Mutlu GY; Kırmızıbekmez H; Aydın H; Çetiner H; Moralıoğlu S; Celayir AC
J Pediatr Endocrinol Metab; 2015 Jan; 28(1-2):207-10. PubMed ID: 25153220
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. A SRY-HMG box frame shift mutation inherited from a mosaic father with a mild form of testicular dysgenesis syndrome in Turner syndrome patient.
Shahid M; Dhillon VS; Khalil HS; Haque S; Batra S; Husain SA; Looijenga LH
BMC Med Genet; 2010 Sep; 11():131. PubMed ID: 20849656
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [Clinical features and Y chromosome abnormalities in children with 45, X/46, XY mosaicism].
Xia JK; Chen C; Hou YQ; Tian FY; Kong XD
Zhonghua Er Ke Za Zhi; 2024 Feb; 62(2):165-169. PubMed ID: 38264817
[No Abstract] [Full Text] [Related]
13. [XY type gonadal dysgenesis, trisomy X and variants].
Kikuchi I; Takeuchi H; Kinoshita K
Nihon Rinsho; 2004 Feb; 62(2):309-12. PubMed ID: 14968537
[TBL] [Abstract][Full Text] [Related]
14. SRY gene increases the risk of developing gonadoblastoma and/or nontumoral gonadal lesions in Turner syndrome.
Bianco B; Lipay M; Guedes A; Oliveira K; Verreschi IT
Int J Gynecol Pathol; 2009 Mar; 28(2):197-202. PubMed ID: 19188812
[TBL] [Abstract][Full Text] [Related]
15. Detection of the SRY gene in patients with Turner Syndrome.
Kurnaz E; Çetinkaya S; Savaş-Erdeve Ş; Aycan Z
J Gynecol Obstet Hum Reprod; 2019 Apr; 48(4):265-267. PubMed ID: 30685428
[TBL] [Abstract][Full Text] [Related]
16. Pathogenetics of 45,X/46,XY gonadal mosaicism.
Reddy KS; Sulcova V
Cytogenet Cell Genet; 1998; 82(1-2):52-7. PubMed ID: 9763660
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesis.
Klee P; Béna F; Birraux J; Dahoun S; Dirlewanger M; Girardin C; Plotton I; Rougemont AL; Morel Y; Schwitzgebel VM
Horm Res Paediatr; 2012; 78(3):188-92. PubMed ID: 22441105
[TBL] [Abstract][Full Text] [Related]
19. Discordant phenotypes and 45,X/46,X,idic(Y).
Kelly TE; Franko JB; Rogol A; Golden WL
J Med Genet; 1998 Oct; 35(10):862-4. PubMed ID: 9783714
[TBL] [Abstract][Full Text] [Related]
20. Presence of Turner stigmata in a case of dysgenetic male pseudohermaphroditism with 45,X/46,X+mar karyotype.
Hashimoto H; Maruyama H; Koshida R; Okuda N; Murayama K; Katsumi T; Watanabe K; Sato T
Arch Dis Child; 1997 Mar; 76(3):268-71. PubMed ID: 9135271
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
