Contribution of whole exome sequencing in the diagnosis of syndromic developmental abnormalities in fetuses
M. Lefebvre,Y. Duffourd,A. Bruel,M. Assoum,P. Kuentz,E. Schaefer, S. El Cheahadeh,M. Antal,J. Mandel,D. Lehalle,N. Jean-Marcais,S. Moutton,C. Philippe,A. Vitobello,F. Tran Mau Them,N. Marle,L. Lambert,P. Jonveaux,B. Foliguet, J. Mazutti,E. Ginglinger,D. Gaillard, C. Poirisier,F. Arbez-Gindre,S. Odent,C. Quelin,M. Fradin,M. Willems,N. Bigi,P. Loget,S. Blesson,C. Francannet,A. Beaufrere,S. Patrier,A. Guerrot,A. Goldenberg,N. Laurent,J. Thevenon,L. Faivre,C. Thauvin-Robinet EUROPEAN JOURNAL OF HUMAN GENETICS(2019)
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