We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleTruncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.AuthorsRoessler, Erich; Yong Ma; Ouspenskaia, Maia V.; Lacbawan, Felicitas; Bendavid, Claude; Dubourg, Christèle; Beachy, Philip A.; Muenke, MaximilianPublicationHuman Genetics, 2009, Vol 125, Issue 4, p393ISSN0340-6717Publication typearticleDOI10.1007/s00439-009-0628-7