T Nagai, R Katoh, T Hasegawa, H Ohashi, Y Fukushima. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChild, PreschoolChromosomes, Human, Pair 13Chromosomes, Human, Pair 20HumansKaryotypingMaleRectum/abnormalitiesSacrum/abnormalitiesTrisomy/genetics
Year: 1994 PMID: 8076416 DOI: 10.1111/j.1399-0004.1994.tb04156.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438