P Harper, J Frézal, M Ferguson-Smith, A Schinzel. Show Affiliations »
Abstract
Mesh: See more » Chromosome DeletionGenetic Diseases, Inborn/geneticsHumansSyndromeTranslocation, Genetic
Year: 1988 PMID: 3203545 DOI: 10.1159/000132670
Source DB: PubMed Journal: Cytogenet Cell Genet ISSN: 0301-0171