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.
243 related articles for article (PubMed ID: 437772)
1. Three cases of sex chromosome mosaicism with a nonfluorescent Y. Madan K; Gooren L; Schoemaker J Hum Genet; 1979 Feb; 46(3):295-304. PubMed ID: 437772 [TBL] [Abstract][Full Text] [Related]
2. [Dysgerminoma and gonadoblastoma in a phenotypic female with 45, X/47, XYY mosaicism]. Tanaka S; Fukue H; Kanaya M; Mizunuma M; Watanabe H; Fujii M; Yamamoto H; Endo T; Hashimoto M Nihon Sanka Fujinka Gakkai Zasshi; 1989 Jun; 41(6):769-72. PubMed ID: 2768969 [No Abstract] [Full Text] [Related]
3. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases. Hsu LY Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637 [TBL] [Abstract][Full Text] [Related]
4. [Men with female karyotypes]. Kövary PM; Niermann H Hautarzt; 1981 Feb; 32(2):63-6. PubMed ID: 7194870 [TBL] [Abstract][Full Text] [Related]
5. Abnormal children of a 47,XYY father. Stoll C; Flori E; Clavert A; Beshara D; Buck P J Med Genet; 1979 Feb; 16(1):66-8. PubMed ID: 157394 [TBL] [Abstract][Full Text] [Related]
7. Cytogenetic and clinical findings in ten 45,X/46,XY patients. Ayuso MC; Ramos MC; Bello MC; Jimenez A; Sanchez Cascos A; Herrera JL Clin Genet; 1984 Apr; 25(4):336-40. PubMed ID: 6713709 [TBL] [Abstract][Full Text] [Related]
8. Acute lymphoblastic leukemia in a 46,XY/47,XYY mosaic male: clonal origin of leukemia in the XY-bearing stem-cell line. Taub JW; Ravindranath Y; Mohamed AN; Wolman SR; Bawle EV Am J Dis Child; 1993 Nov; 147(11):1254-5. PubMed ID: 8237923 [No Abstract] [Full Text] [Related]
9. [Dicentric Y chromosome in a male pseudohermaphrodite 45,X/46,X, dic (Y)/47, XYY]. Roubin M; de Grouchy J; Chauveau P; Rappaport R; Pellerin D Ann Genet; 1977 Sep; 20(3):185-9. PubMed ID: 304702 [TBL] [Abstract][Full Text] [Related]
10. [Study of two brothers with XYY karyotype including one with mosaicism]. Marcoz JP; Bourquin D; Crippa L Arch Genet (Zur); 1978; 51(2):63-70. PubMed ID: 160217 [No Abstract] [Full Text] [Related]
11. Patterns of exchange induced by mitomycin C in C-bands of human chromosomes. II. High frequency of Y-Y exchange in XYY cells. Joseph JL; Brasch JM; Smyth DR Hum Genet; 1982; 62(4):346-8. PubMed ID: 6819988 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Numerical and structural aberrations of human Y chromosome]. Parcheta B Pol Tyg Lek; 1980 Apr; 35(15):543-6. PubMed ID: 6995959 [No Abstract] [Full Text] [Related]
14. Two mosaic cases with nonfluorescent Y chromosome analysed with Y-specific DNA probes. Kałuzewski B; Jakubowski L; Debiec-Rychter M; Grzeschik KH; Limon J; Gibas Z Am J Med Genet; 1988 Nov; 31(3):489-503. PubMed ID: 3228133 [TBL] [Abstract][Full Text] [Related]
15. Ring Y chromosome: cytogenetic and molecular characterization. Wegner RD; Scherer G; Pohlschmidt M; L'Allemand D; Gal A Clin Genet; 1992 Aug; 42(2):71-5. PubMed ID: 1424234 [TBL] [Abstract][Full Text] [Related]
16. Variability in the Y chromosome and variability of human behavior. Dorus E Arch Gen Psychiatry; 1980 May; 37(5):587-94. PubMed ID: 7377917 [TBL] [Abstract][Full Text] [Related]
17. Acute nonlymphocytic leukemia with a translocation (1;3)(p36;q21) in an XYY man. Atichartakarn V; Punyammalee B; Wongsasant B; Jootar S Cancer Genet Cytogenet; 1986 Mar; 21(1):79-83. PubMed ID: 3943075 [TBL] [Abstract][Full Text] [Related]
18. Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism. Fryns JP; Kleczkowska A; Van Den Berghe H Genet Couns; 1990; 1(2):173-7. PubMed ID: 2081001 [No Abstract] [Full Text] [Related]
19. 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]