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pubmed-article:511179pubmed:abstractTextA genetic analysis of human urinary pepsinogen isozymes is presented. Nine discrete phenotypes were identified in a population survey of 215 unrelated Caucasian individuals. The phenotypes were characterized by differences among the staining intensities of the activated group I pepsinogens, Pg 5, Pg 4, Pg 3, and Pg 2. The genetic studies demonstrated that the codominant expression of four alleles, PgA, PgB, PgC and PgD, at a single genetic locus determined the nine phenotypes identified. Linkage analysis excluded close linkage of the Pg locus with the chromosome 6 markers HLA, GLO1, and Bf.lld:pubmed
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pubmed-article:511179pubmed:pagination227-38lld:pubmed
pubmed-article:511179pubmed:dateRevised2010-11-18lld:pubmed
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pubmed-article:511179pubmed:year1979lld:pubmed
pubmed-article:511179pubmed:articleTitleUrinary pepsinogen isozymes: a highly polymorphic locus in man.lld:pubmed
pubmed-article:511179pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:511179pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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