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Titre | Contribution of whole exome sequencing in the diagnosis of syndromic developmental abnormalities in fetuses |
Type de publication | Journal Article |
Year of Publication | 2019 |
Auteurs | Lefebvre 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. |
Journal | EUROPEAN JOURNAL OF HUMAN GENETICS |
Volume | 27 |
Pagination | 358 |
Date Published | JUL |
Type of Article | Meeting Abstract |
ISSN | 1018-4813 |