We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleGermline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndromeAuthorsChampion, KJ; Bunag, C; Estep, AL; Jones, JR; Bolt, CH; Rogers, RC; Rauen, KA; Everman, DBPublicationClinical Genetics, 2011, Vol 79, Issue 5, p468ISSN0009-9163Publication typearticleDOI10.1111/j.1399-0004.2010.01495.x