Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly

Published 2010 View Full Article

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Title
Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly
Authors
Keywords
-
Journal
HUMAN GENETICS
Volume 127, Issue 5, Pages 555-561
Publisher
Springer Nature
Online
2010-02-15
DOI
10.1007/s00439-010-0797-4

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