172 related articles for article (PubMed ID: 18412126)
1. Atypical XX male with the SRY gene located at the long arm of chromosome 1 and a 1qter microdeletion.
Queralt R; Madrigal I; Vallecillos MA; Morales C; Ballescá JL; Oliva R; Soler A; Sánchez A; Margarit E
Am J Med Genet A; 2008 May; 146A(10):1335-40. PubMed ID: 18412126
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. Clinical, cytogenetic, and molecular analysis with 46,XX male sex reversal syndrome: case reports.
Gao X; Chen G; Huang J; Bai Q; Zhao N; Shao M; Jiao L; Wei Y; Chang L; Li D; Yang L
J Assist Reprod Genet; 2013 Mar; 30(3):431-5. PubMed ID: 23378127
[TBL] [Abstract][Full Text] [Related]
5. An XX male with the sex-determining region Y gene inserted in the long arm of chromosome 16.
Dauwerse JG; Hansson KB; Brouwers AA; Peters DJ; Breuning MH
Fertil Steril; 2006 Aug; 86(2):463.e1-5. PubMed ID: 16769064
[TBL] [Abstract][Full Text] [Related]
6. Rare rearrangements: a "jumping satellite" in one family and autosomal location of the SRY gene in an XX male.
Chien SC; Li YC; Ho M; Hsu PC; Teng RH; Lin WD; Tsai FJ; Lin CC
Am J Med Genet A; 2009 Dec; 149A(12):2775-81. PubMed ID: 19921641
[TBL] [Abstract][Full Text] [Related]
7. A comparative genomic hybridization study in a 46,XX male.
Rigola MA; Carrera M; Ribas I; Egozcue J; Miró R; Fuster C
Fertil Steril; 2002 Jul; 78(1):186-8. PubMed ID: 12095512
[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. 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]
10. 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]
11. SRY-positive 46,XX male with cryptorchidism as the only presenting clinical feature.
Moreno-García M; Sánchez Del Pozo J; Gutierrez-Díez P; Gil-Fournier B; Barreiro Miranda E
Urol Int; 2003; 71(2):219-21. PubMed ID: 12890966
[TBL] [Abstract][Full Text] [Related]
12. SRY gene transferred to the long arm of the X chromosome in a Y-positive XX true hermaphrodite.
Margarit E; Coll MD; Oliva R; Gómez D; Soler A; Ballesta F
Am J Med Genet; 2000 Jan; 90(1):25-8. PubMed ID: 10602113
[TBL] [Abstract][Full Text] [Related]
13. Genetic characterization of two 46,XX males without gonadal ambiguities.
Minor A; Mohammed F; Farouk A; Hatakeyama C; Johnson K; Chow V; Ma S
J Assist Reprod Genet; 2008; 25(11-12):547-52. PubMed ID: 18972202
[TBL] [Abstract][Full Text] [Related]
14. A 46,XX SRY-negative man with complete virilization and infertility as the main anomaly.
Valetto A; Bertini V; Rapalini E; Simi P
Fertil Steril; 2005 Jan; 83(1):216-9. PubMed ID: 15652914
[TBL] [Abstract][Full Text] [Related]
15. Unusual maternal uniparental isodisomic x chromosome mosaicism with asymmetric y chromosomal rearrangement.
Lee BY; Kim SY; Park JY; Choi EY; Kim DJ; Kim JW; Ryu HM; Cho YH; Park SY; Seo JT
Cytogenet Genome Res; 2014; 142(2):79-86. PubMed ID: 24434812
[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. Cytogenic and molecular analyses of 46,XX male syndrome with clinical comparison to other groups with testicular azoospermia of genetic origin.
Chiang HS; Wu YN; Wu CC; Hwang JL
J Formos Med Assoc; 2013 Feb; 112(2):72-8. PubMed ID: 23380608
[TBL] [Abstract][Full Text] [Related]
18. 46, XX male sex reversal syndrome: a case report and review of the genetic basis.
Wang T; Liu JH; Yang J; Chen J; Ye ZQ
Andrologia; 2009 Feb; 41(1):59-62. PubMed ID: 19143733
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Normal female phenotype and ovarian development despite the ovarian expression of the sex-determining region of Y chromosome (SRY) in a 46,XX/69,XXY diploid/triploid mosaic child conceived after in vitro fertilization-intracytoplasmic sperm injection.
Oktem O; Paduch DA; Xu K; Mielnik A; Oktay K
J Clin Endocrinol Metab; 2007 Mar; 92(3):1008-14. PubMed ID: 17164312
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
