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.
22. Increasing role of cytogenetics in pediatric practice. Dayakar S; Rani DS; Babu SJ; Srilatha K; Jayanthi U; Goud KI; Jain D; Raina V Genet Test Mol Biomarkers; 2010 Apr; 14(2):197-204. PubMed ID: 20384456 [TBL] [Abstract][Full Text] [Related]
23. Postnatal outcomes of prenatally diagnosed 45,X/46,XX. Tokita MJ; Sybert VP Am J Med Genet A; 2016 May; 170A(5):1196-201. PubMed ID: 26789280 [TBL] [Abstract][Full Text] [Related]
24. Analysis of sex chromosome aneuploidy in 41 patients with Turner syndrome: a study of 'hidden' mosaicism. Fernández-García R; García-Doval S; Costoya S; Pásaro E Clin Genet; 2000 Sep; 58(3):201-8. PubMed ID: 11076042 [TBL] [Abstract][Full Text] [Related]
25. A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes. Mikel'saar AV; Blyumina MG; Kuznetsova LI; Mikel'saar RV; Lur'e IV Sov Genet; 1971 May; 7(5):675-9. PubMed ID: 4272425 [No Abstract] [Full Text] [Related]
26. Chromosome constitution and its bearing on the chromosomal radiosensitivity in man. Sasaki MS; Tonomura A; Matsubara S Mutat Res; 1970 Dec; 10(6):617-33. PubMed ID: 4253911 [No Abstract] [Full Text] [Related]
27. The indications for chromosome analysis as an aid to the clinician. Gordon RR Clin Pediatr (Phila); 1968 Feb; 7(2):83-7. PubMed ID: 4229793 [No Abstract] [Full Text] [Related]
28. The computer analysis of human chromosomes--a suggested new approach. Timson J Int J Biomed Comput; 1970 Jul; 1(3):237-45. PubMed ID: 4255708 [No Abstract] [Full Text] [Related]
29. Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989. Kleczkowska A; Dmoch E; Kubien E; Fryns JP; Van den Berghe H Genet Couns; 1990; 1(3-4):227-33. PubMed ID: 2098046 [TBL] [Abstract][Full Text] [Related]
30. Turner/Down mosaicism. A case report. Jansen S; Kruger AJ; Liebenberg G S Afr Med J; 1991 Jun; 79(12):731-2. PubMed ID: 1828633 [TBL] [Abstract][Full Text] [Related]
31. [Relation of chromosomal aberration and clinical signs in childhood]. Harada Y Kumamoto Igakkai Zasshi; 1969 May; 43(5):387-98. PubMed ID: 4241028 [No Abstract] [Full Text] [Related]
32. 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]
33. Human chromosome abnormalities as related to physical and mental dysfunction. Heller JH J Hered; 1969; 60(5):239-48. PubMed ID: 4244249 [No Abstract] [Full Text] [Related]
35. The role of non-disjunction in aneuploidy in man. An overview. Sankaranarayanan K Mutat Res; 1979 Jun; 61(1):1-28. PubMed ID: 157431 [No Abstract] [Full Text] [Related]
36. The utilization of fluorescent microscopy in routine chromosome analysis. Cullen SJ J Am Med Womens Assoc (1972); 1973 Dec; 28(12):633-8. PubMed ID: 4358510 [No Abstract] [Full Text] [Related]
37. Supernumerary chromosomes in mosaic Turner syndrome. Thong MK; Manonmani V; Norlasiah IS Med J Malaysia; 1996 Dec; 51(4):487-90. PubMed ID: 10968041 [TBL] [Abstract][Full Text] [Related]
38. Gonosomal aneuploidy in anorexia nervosa. Halmi KA; DeBault LE Am J Hum Genet; 1974 Mar; 26(2):195-8. PubMed ID: 4823028 [No Abstract] [Full Text] [Related]
39. 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]