H E Cross. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Anterior Chamber/abnormalitiesChromosomes, Human, 13-15Chromosomes, Human, 16-18Corneal Opacity/geneticsDescemet Membrane/abnormalitiesFemaleGenetic VariationHumansIris/abnormalitiesMaleMarfan Syndrome/geneticsPhenotypeRubella/congenitalSyndromeTooth Abnormalities/geneticsTrisomy
Year: 1979 PMID: 393320
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844