R Proops, A M Taylor, J Insley. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » ChildChild, PreschoolCockayne Syndrome/diagnosisCockayne Syndrome/geneticsDiagnosis, DifferentialDwarfism/geneticsFemaleHumansMalePhenotypeXeroderma Pigmentosum/diagnosis
Year: 1981 PMID: 7277423 PMCID: PMC1048734 DOI: 10.1136/jmg.18.4.288
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318