A. J. M. Hoogeboom
AuthID: R-00F-GC1
1
TÃTULO: The origin of EFNB1 mutations in craniofrontonasal syndrome: Frequent somatic mosaicism and explanation of the paucity of carrier males
AUTORES: Twigg, SRF; Matsumoto, K; Kidd, AMJ; Goriely, A; Taylor, IB; Fisher, RB; Hoogeboom, AJM; Mathijssen, IMJ; Lourenco, MT; Morton, JEV; Sweeney, E; Wilson, LC; Brunner, HG; Mulliken, JB; Wall, SA; Wilkie, AOM;
PUBLICAÇÃO: 2006, FONTE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 78, NÚMERO: 6
AUTORES: Twigg, SRF; Matsumoto, K; Kidd, AMJ; Goriely, A; Taylor, IB; Fisher, RB; Hoogeboom, AJM; Mathijssen, IMJ; Lourenco, MT; Morton, JEV; Sweeney, E; Wilson, LC; Brunner, HG; Mulliken, JB; Wall, SA; Wilkie, AOM;
PUBLICAÇÃO: 2006, FONTE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 78, NÚMERO: 6
