Clinical and molecular characterization of 17q21.31 microdeletion syndrome in 14 French patients with mental retardation-Reference-Cited by-同舟云学术

Clinical and molecular characterization of 17q21.31 microdeletion syndrome in 14 French patients with mental retardation

Published:2011-03 Issue:2 Volume:54 Page:144-151
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Dubourg Christèle,Sanlaville Damien,Doco-Fenzy Martine,Le Caignec Cédric,Missirian Chantal,Jaillard Sylvie,Schluth-Bolard Caroline,Landais Emilie,Boute Odile,Philip Nicole,Toutain Annick,David Albert,Edery Patrick,Moncla Anne,Martin-Coignard Dominique,Vincent-Delorme Catherine,Mortemousque Isabelle,Duban-Bedu Bénédicte,Drunat Sèverine,Beri Mylène,Mosser Jean,Odent Sylvie,David Véronique,Andrieux Joris

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

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5. 17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction;Grisart;J. Med. Genet.,2009

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