P A Benn. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » Cells, CulturedFibroblasts/ultrastructureHumansTranslocation, GeneticWerner Syndrome/genetics
Year: 1985 PMID: 3976660 PMCID: PMC1684541
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025