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A new case of syndromic craniosynostosis with cryptic 19p13.2–p13.13 deletion
Author(s) -
Lysy Philippe A.,
Ravoet Marie,
Wustefeld Sandrine,
Bernard Pierre,
Nassogne MarieCécile,
Wyns Elisabeth,
Sibille Catherine
Publication year - 2009
Publication title -
american journal of medical genetics part a
Language(s) - Portuguese
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.33056
Subject(s) - saint , medicine , library science , art history , history , computer science
A New Case of Syndromic Craniosynostosis With Cryptic 19p13.2–p13.13 Deletion Philippe A. Lysy,* Marie Ravoet, Sandrine Wustefeld, Pierre Bernard, Marie-C ecile Nassogne, Elisabeth Wyns, and Catherine Sibille HPED Department, PEDI Unit, Cliniques Universitaires Saint Luc, Universit e Catholique de Louvain, Brussels, Belgium GMED Department, Center of Medical Genetics, Cliniques Universitaires Saint Luc, Universit e Catholique de Louvain, Brussels, Belgium Obstetrics Service, GYNE Department, Cliniques Universitaires Saint Luc, Universit e Catholique de Louvain, Brussels, Belgium Neuropediatrics Service, NEPE Department, Cliniques Universitaires Saint Luc, Universit e Catholique de Louvain, Brussels, Belgium