Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele. - Suppr | 超能文献

Familial Beckwith-Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele.

作者信息

Percesepe Antonio, Bertucci Emma, Ferrari Paola, Lugli Licia, Ferrari Fabrizio, Mazza Vincenzo, Forabosco Antonino

出版信息

Prenat Diagn. 2008 May;28(5):447-9. doi: 10.1002/pd.1991.

DOI:10.1002/pd.1991

Abstract

摘要

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