J S Glenn, R C Cheung. Show Affiliations »
Abstract
Entities: Chemical Disease
Mesh: See more » FemaleGenetic Testing/methodsHemochromatosis/diagnosisHemochromatosis/geneticsHumansMalePoint MutationSensitivity and Specificity
Year: 1998 PMID: 9655998 PMCID: PMC1305074
Source DB: PubMed Journal: West J Med ISSN: 0093-0415