Contribution of whole exome sequencing in the diagnosis of syndromic developmental abnormalities in fetuses

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TitreContribution of whole exome sequencing in the diagnosis of syndromic developmental abnormalities in fetuses
Type de publicationJournal Article
Year of Publication2019
AuteursLefebvre M., Duffourd Y., Bruel A., Assoum M., Kuentz P., Schaefer E., S. Cheahadeh E, Antal M., Mandel J., Lehalle D., Jean-Marcais N., Moutton S., Philippe C., Vitobello A., F. Them TMau, Marle N., Lambert L., Lambert L., Jonveaux P., Foliguet B., Mazutti J., Ginglinger E., Gaillard D., Poirisier C., Arbez-Gindre F., Odent S., Quelin C., Fradin M., Willems M., Bigi N., Loget P., Blesson S., Francannet C., Beaufrere A., Patrier S., Guerrot A., Goldenberg A., Laurent N., Thevenon J., Faivre L., Thauvin-Robinet C.
JournalEUROPEAN JOURNAL OF HUMAN GENETICS
Volume27
Pagination358
Date PublishedJUL
Type of ArticleMeeting Abstract
ISSN1018-4813