Translocation(X;Y)(p22.33;p11.2) in XX males: Etiology of male phenotype-Reference-Cited by-同舟云学术

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Translocation(X;Y)(p22.33;p11.2) in XX males: Etiology of male phenotype

Published:1982-12 Issue:3 Volume:62 Page:271-276
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Magenis R. E.,Webb M. J.,McKean R. S.,Tomar D.,Allen L. J.,Kammer H.,Van Dyke D. L.,Lovrien E.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00333535.pdf

Reference59 articles.

1. Adam A, Ziprkowski L, Feinstein A, Sanger R, Race RR (1966) Ichthyosis, Xg blood groups, and protan. Lancet I:877

2. �kesson HO, Hagberg B, Wahlstrom J (1980) Y-to-X chromosome translocation observed in two generations. Hum Genet 55:39?42

3. Armendares S, Buentello L, Salamanca F, Cantu-Garza J-M (1972) A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XXqdic, in a patient with features of Turner's syndrome. J Med Genet 9:96?100

4. Arrighi FE, Hsu TC (1971) Localization of heterochromatin in human chromosomes. Cytogenetics 10:81?86

5. Bernstein R, Wagner J, Isdale J, Nurse GT, Lane AB, Jenkins T (1978) X-Y translocation in a retarded phenotypic male. J Med Genet 15: 466?474

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