R J Gorlin. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsDe Lange Syndrome/geneticsFacial Paralysis/geneticsFemaleHumansIntellectual Disability/geneticsKlippel-Feil Syndrome/geneticsMaleOphthalmoplegia/geneticsPectoralis Muscles/abnormalitiesPierre Robin Syndrome/geneticsPrader-Willi Syndrome/geneticsRiskSyndactyly/geneticsSyndrome
Year: 1979 PMID: 230869
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844