S J Funderburk, B F Crandall. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, MultipleBlepharoptosis/geneticsChildChild, PreschoolCraniofacial Dysostosis/geneticsDwarfism/geneticsFemaleFingers/abnormalitiesGenitalia, Male/abnormalitiesHumansInfantInfant, NewbornKaryotypingMalePedigreePhenotypeSyndrome
Year: 1974 PMID: 4430151 DOI: 10.1111/j.1399-0004.1974.tb00639.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438