FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation-Reference-Cited by-同舟云学术

FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation

Published:2009-08-09 Issue:9 Volume:41 Page:1037-1042
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Aldinger Kimberly A,Lehmann Ordan J,Hudgins Louanne,Chizhikov Victor V,Bassuk Alexander G,Ades Lesley C,Krantz Ian D,Dobyns William B,Millen Kathleen J

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.422.pdf

Reference48 articles.

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2. Grinberg, I. et al. Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation. Nat. Genet. 36, 1053–1055 (2004).

3. Parisi, M.A. & Dobyns, W.B. Human malformations of the midbrain and hindbrain: review and proposed classification scheme. Mol. Genet. Metab. 80, 36–53 (2003).

4. Patel, S. & Barkovich, A.J. Analysis and classification of cerebellar malformations. AJNR Am. J. Neuroradiol. 23, 1074–1087 (2002).

5. DeScipio, C. et al. Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome. Am. J. Med. Genet. A. 134, 3–11 (2005).

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