We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMutations in the human SIX3 gene in holoprosencephaly are loss of function.AuthorsDomené, Sabina; Roessler, Erich; El-Jaick, Kenia B.; Snir, Mirit; Brown, Jamie L.; Vélez, Jorge I.; Bale, Sherri; Lacbawan, Felicitas; Muenke, Maximilian; Feldman, BenjaminPublicationHuman Molecular Genetics, 2008, Vol 17, Issue 24, p3919ISSN0964-6906Publication typearticleDOI10.1093/hmg/ddn294