Article info
Developmental defects
Original article
CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome
- Correspondence to Dr Frederic Brioude, Explorations Fonctionnelles Endocriniennes et Biologie Moléculaire, Hôpital Armand Trousseau, 26, avenue du Dr Arnold Netter, Paris 75012, France; frederic.brioude{at}trs.aphp.fr
Citation
CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome
Publication history
- Received March 28, 2013
- Revised August 3, 2013
- Accepted August 28, 2013
- First published September 24, 2013.
Online issue publication
November 05, 2013
Article Versions
- Previous version (24 September 2013).
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