@article{lefebvre:inserm-03231676,
TITLE = {Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations},
AUTHOR = {Lefebvre, M. and Bruel, A. L. and Tisserant, E. and Bourgon, N. and Duffourd, Y. and Collardeau-Frachon, S. and Attie-Bitach, T. and Kuentz, P. and Assoum, M. and Schaefer, E. and El Chehadeh, S. and Antal, M. C. and Kremer, V. and Girard-Lemaitre, F. and Mandel, J. L. and Lehalle, D. and Nambot, S. and Jean-Marcais, N. and Houcinat, N. and Moutton, S. and Marle, N. and Lambert, L. and Jonveaux, P. and Foliguet, B. and Mazutti, J. P. and Gaillard, D. and Alanio, E. and Poirisier, C. and Lebre, A. S. and Aubert-Lenoir, M. and Arbez-Gindre, F. and Odent, S. and Quelin, C. and Loget, P. and Fradin, M. and Willems, M. and Bigi, N. and Perez, M. J. and Blesson, S. and Francannet, C. and Beaufrere, A. M. and Patrier-Sallebert, S. and Guerrot, A. M. and Goldenberg, A. and Brehin, A. C. and Lespinasse, J. and Touraine, R. and Capri, Y. and Saint-Frison, M. H. and Laurent, N. and Philippe, C. and Tran Mau-Them, F. and Thevenon, J. and Faivre, L. and Thauvin-Robinet, C. and Vitobello, A.},
URL = {https://inserm.hal.science/inserm-03231676},
JOURNAL = {Journal of Medical Genetics},
PUBLISHER = {BMJ Publishing Group},
VOLUME = {58},
NUMBER = {6},
PAGES = {400-413},
YEAR = {2021},
MONTH = Jun, DOI = {10.1136/jmedgenet-2020-106867},
KEYWORDS = {genetics ; complex traits ; molecular genetics ; reproductive medicine},
HAL_ID = {inserm-03231676},
HAL_VERSION = {v1},
}