Familial translocation (X;3) (p22.3;p23): chromosomal in situ suppression (CISS) hybridization and inactivation pattern study-Reference-Cited by-同舟云学术

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

Published:2008-06-28 Issue:5 Volume:46 Page:360-363
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Bettio D.,Rizzi N.,Giardino D.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1994.tb04179.x/fullpdf

Reference6 articles.

1. Trisomie partielle pour la partie distale du bras court du chromosome. 3;Ballesta;Ann Génét,1974

2. X-autosome translocations: cytogenetic characteristics and their consequences;Mattei;Hum Genet,1982

3. Failure of X inactivation in the autosomal segment of an X/A translocation;Palmer;Am J Hum Genet,1980

4. Trisomy 3 (p23-pter) resulting from maternal translocation, t(3;4) (p23;q35);Schinzel;Ann Génét,1978

5. High-resolution of human chromosomes;Yunis;Science,1976

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Balanced Reciprocal Translocations Detected at Amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2010-12

2. Familial translocation (X;3)(p22.3;p23): chromosomal in situ suppression (CISS) hybridization and inactivation pattern study;Clinical Genetics;2008-06-28

3. Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation;American Journal of Medical Genetics Part A;2006

4. Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)];American Journal of Medical Genetics;2004

5. Molecular cytogenetic analysis of ade novobalanced X;autosome translocation: Evidence for predominant inactivation of the derivative X chromosome in a girl with multiple malformations;American Journal of Medical Genetics Part A;2003-10-21

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