T F Thurmon, E B DeFraites, E E Anderson. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentAdultAllelesChildFemaleHumansMaleMucopolysaccharidosis II/geneticsPedigreePhenotypeRetinitis Pigmentosa/genetics
Year: 1974 PMID: 4218494
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844