X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00295460.pdf
Reference73 articles.
1. Allderdice PW, Miller OJ, Miller DA, Klinger HP (1978) Spreading of inactivation in an (X;14) translocation. Am J Med Genet 2:233?240
2. Baikie AG, Garson OM, Weste SM, Ferguson J (1966) Numerical abnormalities of the X chromosome. Lancet I:398?400
3. Bartsch-Sandoff M, Terinde R, Wiegelmann W, Scholz W (1976) Karyotyp-Korrelation bei einem 46,Xdel(X)(P22)-Befund. Hum Genet 31:263?270
4. Buckton KE, Jacobs PA, Rae LA, Newton MS (1971) An inherited X-autosome translocation in man. Ann Hum Genet Lond 35:171?178
5. Buhler EM, Jurik LP, Voyame M, Buhler UK (1977) Presumptive evidence of two active X chromosomes in somatic cells of a human female. Nature 265:142?144
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