187 related articles for article (PubMed ID: 12818524)
1. Skewed X-chromosome inactivation pattern in SRY positive XX maleness: a case report and review of literature.
Bouayed Abdelmoula N; Portnoi MF; Keskes L; Recan D; Bahloul A; Boudawara T; Saad A; Rebai T
Ann Genet; 2003; 46(1):11-8. PubMed ID: 12818524
[TBL] [Abstract][Full Text] [Related]
2. Three new 46,XX male patients: a clinical, cytogenetic and molecular analysis.
Grigorescu-Sido A; Heinrich U; Grigorescu-Sido P; Jauch A; Hager HD; Vogt PH; Duncea I; Bettendorf M
J Pediatr Endocrinol Metab; 2005 Feb; 18(2):197-203. PubMed ID: 15751609
[TBL] [Abstract][Full Text] [Related]
3. [Clinical, molecular and cytogenetic studies on 4 patients with 46, XX (SRY positive) male syndrome].
Xia XY; Cui YX; Lu HY; Yang B; Wang GH; Pan LJ; Hou BS; Ge YF; Shao Y; Yao B; Huang YF
Zhonghua Nan Ke Xue; 2007 Dec; 13(12):1094-7. PubMed ID: 18284058
[TBL] [Abstract][Full Text] [Related]
4. Hidden X chromosomal mosaicism in a 46,XX male.
Chernykh VB; Kurilo LF; Shilova NV; Zolotukhina TV; Ryzhkova OP; Bliznetz EA; Polyakov AV
Sex Dev; 2009; 3(4):183-7. PubMed ID: 19752597
[TBL] [Abstract][Full Text] [Related]
5. Clinical, hormonal and cytogenetic evaluation of 46,XX males and review of the literature.
Ergun-Longmire B; Vinci G; Alonso L; Matthew S; Tansil S; Lin-Su K; McElreavey K; New MI
J Pediatr Endocrinol Metab; 2005 Aug; 18(8):739-48. PubMed ID: 16200839
[TBL] [Abstract][Full Text] [Related]
6. Multiscale analysis of SRY-positive 46,XX testicular disorder of sex development: Presentation of nine cases.
Akar OS; Gunes S; Abur U; Altundag E; Asci R; Onat OE; Ozcelik T; Ogur G
Andrologia; 2020 Dec; 52(11):e13739. PubMed ID: 32882067
[TBL] [Abstract][Full Text] [Related]
7. Two males with SRY-positive 46,XX testicular disorder of sex development.
Gunes S; Asci R; Okten G; Atac F; Onat OE; Ogur G; Aydin O; Ozcelik T; Bagci H
Syst Biol Reprod Med; 2013 Feb; 59(1):42-7. PubMed ID: 23110663
[TBL] [Abstract][Full Text] [Related]
8. Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive.
Wu QY; Li N; Li WW; Li TF; Zhang C; Cui YX; Xia XY; Zhai JS
BMC Urol; 2014 Aug; 14():70. PubMed ID: 25169080
[TBL] [Abstract][Full Text] [Related]
9. Localization of the SRY Gene on Chromosome 3 in a Patient with Azoospermia and a Complex Karyotype 45,X/46,X,i(Y)(q10)/46,XX/ 47,XX,i(Y)(q10).
Barnabas LC; Sumathy A; Indumathi MA; Varma TR; Shetty S; Kadandale JS; Kar B
Cytogenet Genome Res; 2018; 156(3):134-139. PubMed ID: 30466086
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Clinical and molecular analysis of XX sex reversed patients.
Kolon TF; Ferrer FA; McKenna PH
J Urol; 1998 Sep; 160(3 Pt 2):1169-72; discussion 1178. PubMed ID: 9719302
[TBL] [Abstract][Full Text] [Related]
12. True hermaphroditism with ambiguous genitalia due to a complicated mosaic karyotype: clinical features, cytogenetic findings, and literature review.
Modan-Moses D; Litmanovitch T; Rienstein S; Meyerovitch J; Goldman B; Aviram-Goldring A
Am J Med Genet A; 2003 Jan; 116A(3):300-3. PubMed ID: 12503111
[TBL] [Abstract][Full Text] [Related]
13. Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome.
Kusz K; Kotecki M; Wojda A; Szarras-Czapnik M; Latos-Bielenska A; Warenik-Szymankiewicz A; Ruszczynska-Wolska A; Jaruzelska J
J Med Genet; 1999 Jun; 36(6):452-6. PubMed ID: 10874632
[TBL] [Abstract][Full Text] [Related]
14. 46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literature.
Li TF; Wu QY; Zhang C; Li WW; Zhou Q; Jiang WJ; Cui YX; Xia XY; Shi YC
BMC Urol; 2014 Dec; 14():104. PubMed ID: 25529318
[TBL] [Abstract][Full Text] [Related]
15. A 45 X male patient with 7q distal deletion and rearrangement with SRY gene translocation: a case report.
Bilen S; Okten A; Karaguzel G; Ikbal M; Aslan Y
Genet Couns; 2013; 24(3):299-305. PubMed ID: 24341145
[TBL] [Abstract][Full Text] [Related]
16. SRY-negative 46,XX male with normal genitals, complete masculinization and infertility.
Rajender S; Rajani V; Gupta NJ; Chakravarty B; Singh L; Thangaraj K
Mol Hum Reprod; 2006 May; 12(5):341-6. PubMed ID: 16556678
[TBL] [Abstract][Full Text] [Related]
17. Cytogenetic and molecular study of a premature male infant with 46,XX derived from ICSI: case report.
Ma S; Tang SS; Yuen BH; Bruyere H; Peñaherrera M; Robinson WP
Hum Reprod; 2003 Nov; 18(11):2298-301. PubMed ID: 14585877
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 46,XX male disorder of sexual development:a case report.
Anık A; Çatlı G; Abacı A; Böber E
J Clin Res Pediatr Endocrinol; 2013; 5(4):258-60. PubMed ID: 24379036
[TBL] [Abstract][Full Text] [Related]
20. The role of the sex-determining region Y gene in the etiology of 46,XX maleness.
Fechner PY; Marcantonio SM; Jaswaney V; Stetten G; Goodfellow PN; Migeon CJ; Smith KD; Berkovitz GD; Amrhein JA; Bard PA
J Clin Endocrinol Metab; 1993 Mar; 76(3):690-5. PubMed ID: 8383144
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
