A new case of syndromic craniosynostosis with cryptic 19p13.2–p13.13 deletion | Zendy

Lysy Philippe A. | Zendy; Ravoet Marie | Zendy; Wustefeld Sandrine | Zendy; Bernard Pierre | Zendy; Nassogne MarieCécile | Zendy; Wyns Elisabeth | Zendy; Sibille Catherine | Zendy

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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

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