Recurrent partial rhombencephalosynapsis and holoprosencephaly in siblings with a mutation of ZIC2
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34029/fullpdf
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4. Holoprosencephaly: Clinical, anatomic, and molecular dimensions;Cohen;Birth Defects Res A Clin Mol Teratol,2006
5. Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3;Delahaye;Eur J Med Genet,2009
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