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4. [Use of molecular cytogenetic techniques for establishing the origin of chromosome markers in patients with Turner phenotype]. Bocian E; Stańczak H; Wiśniewski A; Mazurczak T; Stankiewicz P Pediatr Pol; 1996 Mar; 71(3):203-9. PubMed ID: 8966091 [TBL] [Abstract][Full Text] [Related]
5. [Identification and characterization of marker chromosome in Turner syndrome]. Tan YQ; Cheng DH; DI YF; Li LY; Lu GX Zhonghua Fu Chan Ke Za Zhi; 2007 Oct; 42(10):679-82. PubMed ID: 18241543 [TBL] [Abstract][Full Text] [Related]
6. Identification of the origin of ring/marker chromosomes in patients with Ullrich-Turner syndrome using X and Y specific alpha satellite DNA probes. Tharapel SA; Wilroy RS; Keath AM; Rivas ML; Tharapel AT Am J Med Genet; 1992 Mar; 42(5):720-3. PubMed ID: 1632446 [TBL] [Abstract][Full Text] [Related]
7. [Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype]. Ye ZC; Cai JG; Zhu XY; Zhao R; He XY; Zhong Y; Liu KX; Zhu YM Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):461-4. PubMed ID: 20017317 [TBL] [Abstract][Full Text] [Related]
8. Analysis of Turner syndrome patients within the Jordanian population, with a focus on four patients with Y chromosome abnormalities. Daggag H; Srour W; El-Khateeb M; Ajlouni K Sex Dev; 2013; 7(6):295-302. PubMed ID: 23988405 [TBL] [Abstract][Full Text] [Related]
9. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)]. González-del-Angel A; Blanco B; del Castillo V; Carnevale A Rev Invest Clin; 1995; 47(2):117-25. PubMed ID: 7610280 [TBL] [Abstract][Full Text] [Related]
10. Novel karyotype in the Ullrich-Turner syndrome--45,X/46,X,r(X)/46,X, dic(X)--investigated with fluorescence in situ hybridization. Robson L; Jackson J; Cowell C; Sillence D; Smith A Am J Med Genet; 1994 Apr; 50(3):251-4. PubMed ID: 8042669 [TBL] [Abstract][Full Text] [Related]
11. Y chromosome in Turner syndrome: detection of hidden mosaicism and the report of a rare X;Y translocation case. Bispo AV; Burégio-Frota P; Oliveira dos Santos L; Leal GF; Duarte AR; Araújo J; Cavalcante da Silva V; Muniz MT; Liehr T; Santos N Reprod Fertil Dev; 2014 Oct; 26(8):1176-82. PubMed ID: 25294360 [TBL] [Abstract][Full Text] [Related]
12. A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and mosaicism of 46,X,mar/46,XX. Gray BA; Bent-Williams A; Wolff DJ; Zori RT Clin Genet; 2001 Jul; 60(1):73-6. PubMed ID: 11531974 [TBL] [Abstract][Full Text] [Related]
13. Gonadoblastoma in patients with Ullrich-Turner syndrome. Zelaya G; López Marti JM; Marino R; Garcia de Dávila MT; Gallego MS Pediatr Dev Pathol; 2015; 18(2):117-21. PubMed ID: 25535833 [TBL] [Abstract][Full Text] [Related]
14. Cytogenetic and molecular investigations of Y chromosome sequences and their role in Turner syndrome. Quilter CR; Taylor K; Conway GS; Nathwani N; Delhanty JD Ann Hum Genet; 1998 Mar; 62(Pt 2):99-106. PubMed ID: 9759471 [TBL] [Abstract][Full Text] [Related]
15. Molecular detection of cryptic Y-chromosomal material in patients with Turner syndrome. Cortés-Gutiérrez EI; Herrera-Bartolo R; Dávila-Rodríguez MI; Palacios-Saucedo GC; Vargas-Villarreal J; Romero-Villarreal JB Oncol Rep; 2012 Oct; 28(4):1205-10. PubMed ID: 22824904 [TBL] [Abstract][Full Text] [Related]
16. Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation. Callen DF; Eyre HJ; Dolman G; Garry-Battersby MB; McCreanor JR; Valeba A; McGill JJ J Med Genet; 1995 Feb; 32(2):113-6. PubMed ID: 7760319 [TBL] [Abstract][Full Text] [Related]
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18. Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome. Freriks K; Timmers HJ; Netea-Maier RT; Beerendonk CC; Otten BJ; van Alfen-van der Velden JA; Traas MA; Mieloo H; van de Zande GW; Hoefsloot LH; Hermus AR; Smeets DF Eur J Med Genet; 2013 Sep; 56(9):497-501. PubMed ID: 23933507 [TBL] [Abstract][Full Text] [Related]
19. X microchromosome with additional chromosome anomalies found in Ullrich-Turner syndrome. Wydner KL; Li M; Singer-Granick C; Sciorra LJ; Krueger LJ Am J Med Genet; 1995 Mar; 56(2):141-6. PubMed ID: 7625435 [TBL] [Abstract][Full Text] [Related]
20. Detection of Y chromosomal material in patients with a 45,X karyotype by PCR method. Semerci CN; Satiroglu-Tufan NL; Turan S; Bereket A; Tuysuz B; Yilmaz E; Kayserili H; Karaman B; Semiz S; Duzcan F; Bagci H Tohoku J Exp Med; 2007 Mar; 211(3):243-9. PubMed ID: 17347549 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]