L Owen, B Martin, C E Blank, F Harris. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsAdultAnus, Imperforate/geneticsChromosomes, Human, 21-22 and YChromosomes, Human, 4-5DermatoglyphicsFaceFemaleHumansInfant, NewbornKaryotypingLymphocytes/ultrastructureMaleMicrophthalmos/geneticsSyndromeTranslocation, GeneticTrisomy
Year: 1974 PMID: 4431034 PMCID: PMC1013146 DOI: 10.1136/jmg.11.3.291
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318