E Gazit, R M Goodman, M B Katznelson, Y Rotem. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdultBiopsyChildChild, PreschoolChorioretinitisConnective Tissue/abnormalitiesConsanguinityDermatoglyphicsFemaleGenes, RecessiveHumansInfantIntellectual DisabilityMaleMyopiaPedigreeSkin/pathologySkin Diseases/geneticsSyndrome
Year: 1973 PMID: 4765201 DOI: 10.1111/j.1399-0004.1973.tb01141.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438