We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomaliesAuthorsDemirhan, O; Türkmen, S; Schwabe, G C; Soyupak, S; Akgül, E; Taştemir, D; Karahan, D; Mundlos, S; Lehmann, KPublicationJournal of Medical Genetics (JMG), 2005, Vol 42, Issue 4, p314ISSN0022-2593Publication typearticle