K Fried, G Mundel. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdultEgyptFemaleFingers/abnormalitiesGene FrequencyGenes, DominantHumansInfant, NewbornIsraelJewsMaleMarfan Syndrome/complicationsMarfan Syndrome/geneticsPedigreePhenotypeSyndactyly/complicationsSyndactyly/geneticsToes/abnormalities
Year: 1974 PMID: 4366482 PMCID: PMC1013109 DOI: 10.1136/jmg.11.2.141
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318