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Familial Beckwith–Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele
Author(s) -
Percesepe Antonio,
Bertucci Emma,
Ferrari Paola,
Lugli Licia,
Ferrari Fabrizio,
Mazza Vincenzo,
Forabosco Antonino
Publication year - 2008
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.1991
Subject(s) - medicine , obstetrics and gynaecology , omphalocele , pediatrics , pregnancy , biology , genetics , fetus
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