Genotype and phenotype features of 22 patients with intellectual disability caused by MED13L variations
T. Smol,F. Petit,B. Gerard,B. Keren,C. Thuillier, D. Sanlavile, E. Boudry-Labis,G. Lesca,D. Heron,L. Faivre,C. Nava,P. Kuentz,F. Devillard,P. Saugier-Veber,A. Guerrot,A. Verloes,C. Coubes,R. Caumes,A. Dieux-Coeslier,O. Boute-Benejean, S. Bouquillon,A. Afenjar, M. Field,Y. A. Zarate, I. Marey, E. Lapi, E. Fassi, C. Couton,T. Roscioli, M. Doco-Fenzy, N. Porchet, C. Roche-Lestienne,S. Manouvrier-Hanu,A. Piton, J. Ghoumid EUROPEAN JOURNAL OF HUMAN GENETICS（2018）
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