A I Taylor. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, MultipleChromosome Aberrations/pathologyChromosome DisordersChromosomes, Human, 16-18DermatoglyphicsGonads/pathologyHumansInfant, NewbornKaryotypingMaleTrisomy
Year: 1971 PMID: 5098068 PMCID: PMC1468978 DOI: 10.1136/jmg.8.1.123
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318