These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
235 related articles for article (PubMed ID: 15579656)
1. Fate of SRY, PABY, DYS1, DYZ3 and DYZ1 loci in Indian patients harbouring sex chromosomal anomalies. Bashamboo A; Rahman MM; Prasad A; Chandy SP; Ahmad J; Ali S Mol Hum Reprod; 2005 Feb; 11(2):117-27. PubMed ID: 15579656 [TBL] [Abstract][Full Text] [Related]
2. Two new novel point mutations localized upstream and downstream of the HMG box region of the SRY gene in three Indian 46,XY females with sex reversal and gonadal tumour formation. Shahid M; Dhillion VS; Jain N; Hedau S; Diwakar S; Sachdeva P; Batra S; Das BC; Husain SA Mol Hum Reprod; 2004 Jul; 10(7):521-6. PubMed ID: 15155818 [TBL] [Abstract][Full Text] [Related]
3. Histologic analysis of gonadal tissue in patients with Ullrich-Turner syndrome and derivative Y chromosomes. Horn LC; Limbach A; Hoepffner W; Tröbs RB; Keller E; Froster UG; Richter CE; Jakubiczka S Pediatr Dev Pathol; 2005; 8(2):197-203. PubMed ID: 15747103 [TBL] [Abstract][Full Text] [Related]
4. A point mutation, R59G, within the HMG-SRY box in a female 45,X/46,X, psu dic(Y)(pter-->q11::q11-->pter). Fernandez R; Marchal JA; Sanchez A; Pasaro E Hum Genet; 2002 Sep; 111(3):242-6. PubMed ID: 12215836 [TBL] [Abstract][Full Text] [Related]
5. Screening for mutations in the SRY gene in patients with mixed gonadal dysgenesis or with Turner syndrome and Y mosaicism. Canto P; Galicia N; Söderlund D; Escudero I; Méndez JP Eur J Obstet Gynecol Reprod Biol; 2004 Jul; 115(1):55-8. PubMed ID: 15223166 [TBL] [Abstract][Full Text] [Related]
6. Tandem duplication and copy number polymorphism of the SRY gene in patients with sex chromosome anomalies and males exposed to natural background radiation. Premi S; Srivastava J; Chandy SP; Ahmad J; Ali S Mol Hum Reprod; 2006 Feb; 12(2):113-21. PubMed ID: 16510537 [TBL] [Abstract][Full Text] [Related]
7. [Screening for Y chromosome sequences in patients with Turner syndrome]. Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154 [TBL] [Abstract][Full Text] [Related]
8. Clinical implications of the detection of Y-chromosome mosaicism in Turner's syndrome: report of 3 cases. Bianco B; Nunes Lipay MV; Guedes AD; Verreschi IT Fertil Steril; 2008 Oct; 90(4):1197.e17-20. PubMed ID: 18295215 [TBL] [Abstract][Full Text] [Related]
9. Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis. Aktas D; Alikasifoglu M; Gonc N; Senocak ME; Tuncbilek E Eur J Med Genet; 2006; 49(2):141-9. PubMed ID: 16530711 [TBL] [Abstract][Full Text] [Related]
10. Molecular identification of chromosome Y sequences in Brazilian patients with Turner syndrome. Araujo C; Galera MF; Galera BB; Silvestre FG; Medeiros SF Gynecol Endocrinol; 2008 Dec; 24(12):713-7. PubMed ID: 19172542 [TBL] [Abstract][Full Text] [Related]
12. Detection of Y-chromosomal DNA with marker chromosomes in Turner's syndrome. Kuo PL; Wu RC; Tzeng CC; Lin SJ; Liu SS; Huang KE J Formos Med Assoc; 1995 Aug; 94(8):474-80. PubMed ID: 7549576 [TBL] [Abstract][Full Text] [Related]
13. [An investigation of small marker chromosome in eight Turner syndrome patients by fluorescence in situ hybridization and DNA analysis]. Hu X; Zhu B; Hu B; Lin H; Shu D; Li C; Liu X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Dec; 16(6):392-4. PubMed ID: 10581353 [TBL] [Abstract][Full Text] [Related]
14. [Analysis of specific sequences in female patients with Turner syndrome--initial study]. Vodicka R; Vrtĕl R; Adamová K; Zapletalová J; Lebl J; Santavý J; Santavá A; Kolárová J; Konvalinka D; Krejciríková E Cas Lek Cesk; 2002 Jul; 141(13):421-4. PubMed ID: 12238030 [TBL] [Abstract][Full Text] [Related]
15. [Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization]. Liang Y; Luo XP Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):435-7. PubMed ID: 16086285 [TBL] [Abstract][Full Text] [Related]
16. A mutation in the 5' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism. Canto P; de la Chesnaye E; López M; Cervantes A; Chávez B; Vilchis F; Reyes E; Ulloa-Aguirre A; Kofman-Alfaro S; Méndez JP J Clin Endocrinol Metab; 2000 May; 85(5):1908-11. PubMed ID: 10843173 [TBL] [Abstract][Full Text] [Related]
17. [Genotypic sex and phenotypic sex: clinical, biochemical and molecular aspects in a patient with male hypogonadism and 46XX-45XO karyotype]. Torre R; Savino A; Venturi P; Taverna R; Triacca R; Coli A; Bernasconi D; Del Monte P; Marugo M Recenti Prog Med; 2001 Dec; 92(12):747-50. PubMed ID: 11822095 [TBL] [Abstract][Full Text] [Related]
18. Presence of Y chromosome sequences and their effect on the phenotype of six patients with Y chromosome anomalies. Shankman S; Spurdle AB; Morris D; Rosendorff J; Marques I; Bernstein R; Ramsay M Am J Med Genet; 1995 Jan; 55(3):269-75. PubMed ID: 7726221 [TBL] [Abstract][Full Text] [Related]
19. Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype. Caglayan AO; Demiryilmaz F; Kendirci M; Ozyazgan I; Akalin H; Bittmann S Genet Couns; 2009; 20(2):173-9. PubMed ID: 19650415 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]