We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitlePhenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human developmentAuthorsSanlaville, D; Etchevers, H C; Gonzales, M; Martinovic, J; Clément-Ziza, M; Delezoide, A-L; Aubry, M-C; Pelet, A; Chemouny, S; Cruaud, C; Audollent, S; Esculpavit, C; Goudefroye, G; Ozilou, C; Fredouille, C; Joye, N; Morichon-Delvallez, N; Dumez, Y; Weissenbach, J; Munnich, A; Amiel, J; Encha-Razavi, F; Lyonnet, S; Vekemans, M; Attié-Bitach, TPublicationJournal of Medical Genetics (JMG), 2006, Vol 43, Issue 3, p211ISSN0022-2593Publication typearticle