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TITLE: The origin of EFNB1 mutations in craniofrontonasal syndrome: Frequent somatic mosaicism and explanation of the paucity of carrier males
AUTHORS: 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;
PUBLISHED: 2006, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 78, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef