Mutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features

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TitreMutations in the ERCC2 (XPD) gene associated with severe fetal ichthyosis and dysmorphic features
Type de publicationJournal Article
Year of Publication2016
AuteursMiguet M, Thevenon J, Laugel V, Lefebvre M, Bourchany A, Riviere J-B, Duffourd Y, Schaefer E, Antal MCristina, Abida R, Weingertner A-S, Kremer V, Vabres P, Morice-Picard F, Gonzales M, Lipsker D, Fraitag S, Mandel J-L, Chelly J, Dollfus H, Faivre L, Thauvin-Robinet C, Calmels N, Chehadeh SEl
JournalPRENATAL DIAGNOSIS
Volume36
Pagination1276-1279
Date PublishedDEC
Type of ArticleEditorial Material
ISSN0197-3851
DOI10.1002/pd.4965