S L Wenger. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Chromosomes, Human, Pair 15/ultrastructureFemaleHumansMaleMeiosisPrader-Willi Syndrome/geneticsTranslocation, Genetic
Year: 1991 PMID: 1778009 DOI: 10.1111/j.1399-0004.1991.tb03121.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438