Genetic linkage between hereditary hemochromatosis and HLA
about
A highly polymorphic locus in human DNASegregation and linkage studies of plasma dopamine-beta-hydroxylase (DBH), erythrocyte catechol-O-methyltransferase (COMT), and platelet monoamine oxidase (MAO): possible linkage between the ABO locus and a gene controlling DBH activityConstruction of a genetic linkage map in man using restriction fragment length polymorphismsEstimation of segregation and linkage parameters in simulated data. II. Simultaneous estimation with one linked markerSegregation of genetic hemochromatosis indexed by latent capacity of transferrinThe use of association data to identify family members at high risk for marker-linked diseases.The affected sib method. III. Selection and recombination.Segregation analysis incorporating linkage markers. I. Single-locus models with an application to type I diabetes.Genetic distances between the Utah Mormons and related populationsGenetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) informationMapping the locus for hereditary hemochromatosis: localization between HLA-B and HLA-A.Some epistatic two-locus models of disease. I. Relative risks and identity-by-descent distributions in affected sib pairsSome epistatic two-locus models of disease. II. The confounding of linkage and association.A simple method for testing two-locus models of inheritance.Two previously undetected variants of glutamic-pyruvic transaminase found by acidic polyacrylamide gel electrophoresis.Major locus analysis for quantitative traits.Chromosomal localization of nucleic acid-binding proteins by affinity mapping: assignment of the IRE-binding protein gene to human chromosome 9Estimating the power of a proposed linkage study for a complex genetic trait.The significance of haemochromatosis gene mutations in the general population: implications for screening.Articular manifestations of systemic diseasesThe human genome through the eyes of Mercator and Vesalius.Association of HLA-linked hemochromatosis with idiopathic refractory sideroblastic anemia.Assessing the role of HLA-linked and unlinked determinants of disease.A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA asA sib-pair strategy for the use of restriction fragment length polymorphisms to study the mode of transmission of type II diabetes.
P2860
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P2860
Genetic linkage between hereditary hemochromatosis and HLA
description
1979 nî lūn-bûn
@nan
1979 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1979 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
name
Genetic linkage between hereditary hemochromatosis and HLA
@ast
Genetic linkage between hereditary hemochromatosis and HLA
@en
type
label
Genetic linkage between hereditary hemochromatosis and HLA
@ast
Genetic linkage between hereditary hemochromatosis and HLA
@en
prefLabel
Genetic linkage between hereditary hemochromatosis and HLA
@ast
Genetic linkage between hereditary hemochromatosis and HLA
@en
P2093
P2860
P1476
Genetic linkage between hereditary hemochromatosis and HLA
@en
P2093
Cannings C
Carmelli D
Cartwright G
Skolnick M
P2860
P304
P407
P577
1979-09-01T00:00:00Z