K Willson, J Q Miller, W Wilson, G Schott. Show Affiliations »
Abstract
Mesh: See more » AllelesChromosome Aberrations/geneticsChromosome DisordersChromosomes, Human, 13-15HumansPentosyltransferases/geneticsPurine-Nucleoside Phosphorylase/geneticsTrisomy
Substances: See more » PentosyltransferasesPurine-Nucleoside Phosphorylase
Year: 1981 PMID: 6787202 PMCID: PMC1048696 DOI: 10.1136/jmg.18.2.158-a
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318