Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria-Reference-Cited by-同舟云学术

Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria

Published:2013-10-03 Issue:10 Volume:9 Page:e1003823
ISSN:1553-7404
Container-title:PLoS Genetics
language:en
Short-container-title:PLoS Genet

Author:

Sajan Samin A.,Fernandez Liliana,Nieh Sahar Esmaeeli,Rider Eric,Bukshpun Polina,Wakahiro Mari,Christian Susan L.,Rivière Jean-Baptiste,Sullivan Christopher T.,Sudi Jyotsna,Herriges Michael J.,Paciorkowski Alexander R.,Barkovich A. James,Glessner Joseph T.,Millen Kathleen J.,Hakonarson Hakon,Dobyns William B.,Sherr Elliott H.

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics(clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference69 articles.

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4. Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2;WB Dobyns;Am J Med Genet A,2008

5. Human malformations of the midbrain and hindbrain: review and proposed classification scheme;MA Parisi;Mol Genet Metab,2003

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