Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01684.x/fullpdf
Reference24 articles.
1. Holoprosencephaly: recommendations for diagnosis and management.;Kauvar;Curr Opin Pediatr,2010
2. Holoprosencephaly.;Dubourg;Orphanet J Rare Dis,2007
3. Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.;Brown;Nat Genet,1998
4. The ZIC gene family in development and disease.;Grinberg;Clin Genet,2005
5. Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.;Solomon;J Med Genet,2010
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