J Francois. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AtrophyCataract/congenitalConsanguinityDiagnosis, DifferentialDwarfism/geneticsFemaleHallermann's Syndrome/geneticsHumansHypotrichosis/geneticsMaleMandibulofacial Dysostosis/geneticsMicrophthalmos/geneticsPedigreeSkin/pathology
Year: 1982 PMID: 6756501
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844