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

Prenatal diagnosis - 1 May 2008

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

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PMID: 18395877
DOI: 10.1002/pd.1991

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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