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A locus for Fanconi anemia on 16q determined by homozygosity mapping.
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.
Radiation hybrid map of the mouse genome.
Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci.
Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height.
Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33.
The appropriate threshold for declaring linkage when allowing sex-specific recombination rates.
Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat.
Absence of linkage between inflammatory bowel disease and selected loci on chromosomes 3, 7, 12, and 16.
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
Characterization of the MODY3 phenotype. Early-onset diabetes caused by an insulin secretion defect.
High-resolution genetic mapping of complex traits.
Mapping mendelian factors underlying quantitative traits using RFLP linkage maps.
Rapid multipoint linkage analysis of recessive traits in nuclear families, including homozygosity mapping.
Parametric and nonparametric linkage analysis: a unified multipoint approach.
Quantitative locus analysis of airway hyperresponsiveness in A/J and C57BL/6J mice.
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results.
Genomewide scan of multiple sclerosis in Finnish multiplex families.