Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleCongenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter.AuthorsAngelicheva D; Turnev I; Dye D; Chandler D; Thomas PK; Kalaydjieva LPublicationEuropean journal of human genetics : EJHG, 1999, Vol 7, Issue 5, p560ISSN1018-4813Publication typearticleDOI10.1038/sj.ejhg.5200319