Heterozygous deletion of the Williams–Beuren syndrome critical interval in mice recapitulates most features of the human disorder-Reference-Cited by-同舟云学术

Heterozygous deletion of the Williams–Beuren syndrome critical interval in mice recapitulates most features of the human disorder

Published:2014-07-15 Issue:24 Volume:23 Page:6481-6494
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Segura-Puimedon Maria,Sahún Ignasi,Velot Emilie,Dubus Pierre,Borralleras Cristina,Rodrigues Ana J.,Valero María C.,Valverde Olga,Sousa Nuno,Herault Yann,Dierssen Mara,Pérez-Jurado Luis A.,Campuzano Victoria

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/23/24/6481/13907505/ddu368.pdf

Reference62 articles.

1. Prevalence estimation of Williams syndrome;Stromme;J. Child. Neurol.,2002

2. Williams-Beuren syndrome: a model of recurrent genomic mutation;Perez Jurado;Horm. Res.,2003

3. The genomic basis of the Williams-Beuren syndrome;Schubert;Cell. Mol. Life Sci.,2009

4. Mutational mechanisms of Williams-Beuren syndrome deletions;Bayes;Am. J. Hum. Genet.,2003

5. A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23;Peoples;Am. J. Hum. Genet.,2000

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