Targeted loss of the ATR-X syndrome protein in the limb mesenchyme of mice causes brachydactyly-Reference-Cited by-同舟云学术

Targeted loss of the ATR-X syndrome protein in the limb mesenchyme of mice causes brachydactyly

Published:2013-07-25 Issue:24 Volume:22 Page:5015-5025
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Solomon Lauren A.,Russell Bailey A.,Watson L. Ashley,Beier Frank,Bérubé Nathalie G.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/22/24/5015/14140240/ddt351.pdf

Reference43 articles.

1. Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome);Gibbons;Cell,1995

2. Molecular-clinical spectrum of the ATR-X syndrome;Gibbons;Am. J. Hum. Genet.,2000

3. Clinical and hematologic aspects of the X-linked α-thalassemia/mental retardation syndrome (ATR-X);Gibbons;Am. J. Hum. Genet.,1995

4. Non-skewed X-inactivation may cause mental retardation in a female carrier of X-linked α-thalassemia/mental retardation syndrome (ATR-X): X-inactivation study of nine female carriers of ATR-X;Wada;Am. J. Hum. Genet.,2005

5. Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation;Gibbons;Nat. Genet.,2000

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