Familial Beckwith–Wiedemann syndrome due toCDKN1C mutation manifesting with recurring omphalocele

Published 2008 View Full Article

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Title
Familial Beckwith–Wiedemann syndrome due toCDKN1C mutation manifesting with recurring omphalocele
Authors
Keywords
-
Journal
PRENATAL DIAGNOSIS
Volume 28, Issue 5, Pages 447-449
Publisher
Wiley
Online
2008-04-08
DOI
10.1002/pd.1991

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