J P Fryns1. Show Affiliations » 1. Centre for Human Genetics, University of Leuven, Belgium.
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsFingers/abnormalitiesGenes, DominantGenetic VariationHumansScalp/abnormalitiesSkull/abnormalitiesSyndromeToes/abnormalities
Year: 1987 PMID: 3656372 PMCID: PMC1050207 DOI: 10.1136/jmg.24.8.493
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318