Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci-Reference-Cited by-同舟云学术

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

Published:2009-09-14 Issue:24 Volume:18 Page:4724-4733
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Azzi Salah,Rossignol Sylvie,Steunou Virginie,Sas Theo,Thibaud Nathalie,Danton Fabienne,Le Jule Maryline,Heinrichs Claudine,Cabrol Sylvie,Gicquel Christine,Le Bouc Yves,Netchine Irene

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/18/24/4724/17247840/ddp435.pdf

Reference49 articles.

1. Identification of novel imprinted genes in a genome-wide screen for maternal methylation;Smith;Genome Res.,2003

2. Mechanisms regulating imprinted genes in clusters;Edwards;Curr. Opin. Cell. Biol.,2007

3. Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals;Jaenisch;Nat. Genet.,2003

4. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest;Lefebvre;Nat. Genet.,1998

5. DNA methylation and human disease;Robertson;Nat. Rev. Genet.,2005

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