R Happle. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChromosome DeletionChromosomes, Human, Pair 3FemaleGenetic Linkage/geneticsHumansSkin Diseases/genetics
Year: 1990 PMID: 2227944 DOI: 10.1007/bf00194239
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132