R S Wilroy, R L Summitt, R E Tipton, P A Primm, P R Martens. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdultChildCraniofacial Dysostosis/geneticsFemaleHumansIntellectual Disability/geneticsMaleNoonan Syndrome/classificationNoonan Syndrome/geneticsPedigreePhenotype
Year: 1979 PMID: 526584
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844