K H Halloran, W R Breg, M J Mahoney. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » Abnormalities, Multiple/geneticsAneuploidyChromosomes, Human, 21-22 and YFemaleHeart Defects, CongenitalHumansHypertelorism/geneticsInfantIntellectual Disability/geneticsKaryotypingMicrognathism/genetics
Year: 1974 PMID: 4443988 PMCID: PMC1013214 DOI: 10.1136/jmg.11.4.386
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318