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

标题
Familial Beckwith–Wiedemann syndrome due toCDKN1C mutation manifesting with recurring omphalocele
作者
关键词
-
出版物
PRENATAL DIAGNOSIS
Volume 28, Issue 5, Pages 447-449
出版商
Wiley
发表日期
2008-04-08
DOI
10.1002/pd.1991

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