F Andiran, F C Tanyel, A Hiçsönmez. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Eye Abnormalities/geneticsHumansInfant, NewbornMaleSkin Abnormalities/geneticsSyndactyly/geneticsSyndromeUrethra/abnormalities
Year: 1999 PMID: 10051174 DOI: 10.1002/(sici)1096-8628(19990212)82:4<359::aid-ajmg17>3.0.co;2-q
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299