Molecular cytogenetic analysis of ade novobalanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations-Reference-Cited by-同舟云学术

Molecular cytogenetic analysis of ade novobalanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations

Published:2003-10-21 Issue:3 Volume:126A Page:229-236
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Gläser B.,Shirneshan K.,Bink K.,Wirth J.,Kehrer-Sawatzki H.,Bartz U.,Zoll B.,Bohlander Stefan K.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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3. Familial translocation (X;3) (p22.3;p23): chromosomal in situ suppression (CISS) hybridization and inactivation pattern study;Bettio;Clin Genet,1994

4. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype;Canun;Am J Med Genet,1998

5. A novel class of zinc finger/leucine zipper genes identified from the molecular cloning of the t(10;11) translocation in acute leukemia;Chaplin;Blood,1995

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