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Familial Beckwith–Wiedemann syndrome due to CDKN1C mutation manifesting with recurring omphalocele
Antonio Percesepe, Emma Bertucci, Paola Ferrari, Licia Lugli, Fabrizio Ferrari, Vincenzo Mazza, Antonino ForaboscoVolume:
28
Year:
2008
Language:
english
Pages:
3
DOI:
10.1002/pd.1991
File:
PDF, 71 KB
english, 2008