154 related articles for article (PubMed ID: 11170081)
1. 47,XXX male: A clinical and molecular study.
Ogata T; Matsuo M; Muroya K; Koyama Y; Fukutani K
Am J Med Genet; 2001 Feb; 98(4):353-6. PubMed ID: 11170081
[TBL] [Abstract][Full Text] [Related]
2. An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.
Annerén G; Andersson M; Page DC; Brown LG; Berg M; Läckgren G; Gustavson KH; de la Chapelle A
Am J Hum Genet; 1987 Oct; 41(4):594-604. PubMed ID: 2889356
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. An SRY-negative 47,XXY mother and daughter.
Röttger S; Schiebel K; Senger G; Ebner S; Schempp W; Scherer G
Cytogenet Cell Genet; 2000; 91(1-4):204-7. PubMed ID: 11173857
[TBL] [Abstract][Full Text] [Related]
6. Partial disomy of Xp and the presence of SRY in a phenotypic female.
Bajalica S; Blennow E; Tşezou A; Galla-Voumvouraki A; Alevizaki M; Sinaniotis C; Kitsiou-Tzeli S
J Med Genet; 1995 Dec; 32(12):987-90. PubMed ID: 8825932
[TBL] [Abstract][Full Text] [Related]
7. 45,X/46,X,idic(Yq) mosaicism: clinical, cytogenetic, and molecular studies in four individuals.
Teraoka M; Narahara K; Yokoyama Y; Tsuji K; Kikkawa K; Ito S; Koyama K; Seino Y
Am J Med Genet; 1998 Aug; 78(5):424-8. PubMed ID: 9714008
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Sex chromosome mosaicism in gonads of a fetus with cystic hygroma and deletion of the short arm of Y chromosome including loss of SRY.
Aviv H; Heller D; Fajardo A; Hoot A; Mavaro L
Am J Med Genet; 2001 Aug; 102(2):157-60. PubMed ID: 11477609
[TBL] [Abstract][Full Text] [Related]
10. Localization of SRY by primed in situ labeling in XX and XY sex reversal.
Kadandale JS; Wachtel SS; Tunca Y; Wilroy RS; Martens PR; Tharapel AT
Am J Med Genet; 2000 Nov; 95(1):71-4. PubMed ID: 11074498
[TBL] [Abstract][Full Text] [Related]
11. Two SRY-negative XX male brothers without genital ambiguity.
Zenteno JC; López M; Vera C; Méndez JP; Kofman-Alfaro S
Hum Genet; 1997 Oct; 100(5-6):606-10. PubMed ID: 9341880
[TBL] [Abstract][Full Text] [Related]
12. Localization of the sex-determining region-Y gene in XX males.
Suzuki Y; Sasagawa I; Yazawa H; Tateno T; Nakada T; Saito H; Hiroi M
Arch Androl; 2000; 44(2):133-6. PubMed ID: 10746870
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. A rare case of 46,XX true hermaphroditism with hidden mosaicism with sex-determining region Y chromosome-bearing cells in the gonads.
Inoue H; Nomura M; Yanase T; Ichino I; Goto K; Ikuyama S; Takayanagi R; Nawata H
Intern Med; 1998 May; 37(5):467-71. PubMed ID: 9652903
[TBL] [Abstract][Full Text] [Related]
16. Xp;Yp translocation inherited from the father in an SRY, RBM, and TSPY positive true hermaphrodite with oligozoospermia.
Jakubowski L; Jeziorowska A; Constantinou M; Helszer Z; Baumstark A; Vogel W; Mikiewicz-Syguła D; Kaułzewski B
J Med Genet; 2000 Oct; 37(10):E28. PubMed ID: 11015460
[No Abstract] [Full Text] [Related]
17. 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]
18. Development in a 46 XX boy with positive SRY gene.
Rego A; Margarit E; Estivill X; Regal M; García-Mayor RV
J Pediatr Endocrinol Metab; 1996; 9(6):623-6. PubMed ID: 9004179
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of a 45,X male with a SRY-bearing chromosome 21.
Nataf V; Senat MV; Albert M; Bidat L; de Mazancourt P; Roume J; Allard L; Le Tessier D; Ville Y; Selva J
Prenat Diagn; 2002 Aug; 22(8):675-80. PubMed ID: 12210575
[TBL] [Abstract][Full Text] [Related]
20. Cytogenetic and molecular characterization of two isodicentric Y chromosomes.
Stankiewicz P; Hélias-Rodzewicz Z; Jakubów-Durska K; Bocian E; Obersztyn E; Rappold GA; Mazurczak T
Am J Med Genet; 2001 Jun; 101(1):20-5. PubMed ID: 11343332
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]