WNT10A mutations: refining genotype, phenotype, penetrance, clinical variability and inheritance manner
O. Patat,I. Bailleul-Forestier,J. Plaisancie,D. Bonneau,E. Colin,C. Colson,M. Cordier,C. Coubes, F. Demurger,A. Dieux-Coeslier, M. Fradin,M. Gerard,A. Goldenberg,B. Isidor,H. Journel,D. Lacombe,M. Lebrun, D. Martin-Coignard,M. Nizon,S. Odent, F. Petit, N. Philip,J. Piard, G. Plessis,A. Putoux,C. Quelin, J. Thevenon,A. Toutain, C. Vanleberghe,A. Verloes, C. Vincent-Delorme, Y. Capri, F. Vaysse, P. Calvas, N. Chassaing EUROPEAN JOURNAL OF HUMAN GENETICS（2019）
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