Phenotype Severity and Genetic Variation at the Disease Locus
Double Heterozygosity with Mutations Involving both the GJB2 and GJB6 Genes is a Possible, but very Rare, Cause of Congenital Deafness in the Czech Population
Comprehensive Cystic Fibrosis Mutation Epidemiology and Haplotype Characterization in a Southern Italian Population
The Contribution of Genetic and Environmental Factors to Quantitative Variability of Erythrocyte Membrane Proteins in Primary Hypotension
β2-Adrenergic Receptor Gene Variations Associated with Stage-2 Hypertension in Northern Han Chinese
Linkage Analysis of Chromosome 1 with Essential Hypertension and Blood Pressure Quantitative Traits in Chinese Families
Genetic Heterogeneity of Beta Thalassemia in Lebanon Reflects Historic and Recent Population Migration
Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups
Genetic Association Studies in Complex Disease
Fine Mapping Functional Sites or Regions from Case-Control Data Using Haplotypes of Multiple Linked SNPs
Linkage Analysis of Affected Sib Pairs Allowing for Parent-of-Origin Effects
The use of Allelic Expression Differences to Ascertain Functional Polymorphisms Acting in cis