Submicroscopic Deletion in Patients with Williams-Beuren Syndrome Influences Expression Levels of the Nonhemizygous Flanking Genes-Reference-Cited by-同舟云学术

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Submicroscopic Deletion in Patients with Williams-Beuren Syndrome Influences Expression Levels of the Nonhemizygous Flanking Genes

Published:2006-08 Issue:2 Volume:79 Page:332-341
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Merla Giuseppe,Howald Cédric,Henrichsen Charlotte N.,Lyle Robert,Wyss Carine,Zabot Marie-Thérèse,Antonarakis Stylianos E.,Reymond Alexandre

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference57 articles.

1. Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease;Shaw;Hum Mol Genet,2004

2. Large-scale copy number polymorphism in the human genome;Sebat;Science,2004

3. Detection of large-scale variation in the human genome;Iafrate;Nat Genet,2004

4. Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates;Frazer;Genome Res,2003

5. Analysis of primate genomic variation reveals a repeat-driven expansion of the human genome;Liu;Genome Res,2003

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