Familial Beckwith–Wiedemann syndrome due to CDKN1C mutation...

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 Forabosco
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Volume:
28
Year:
2008
Language:
english
Pages:
3
DOI:
10.1002/pd.1991
File:
PDF, 71 KB
english, 2008
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