Nucleotide Sequence Analyses of Human Complement 6 (C6) Gene Suggest Balancing Selection
Analysis of Dystrophin Gene Deletions Indicates that the Hinge III Region of the Protein Correlates with Disease Severity
Simultaneous Selection of the Wild-type Genotypes of the G894T and 4B/ 4A Polymorphisms of NOS3 Associate with High-altitude Adaptation
Wilson Disease
The Effect of Genetic Drift in a Young Genetically Isolated Population
Power and Related Statistical Properties of Conditional Likelihood Score Tests for Association Studies in Nuclear Families with Parental Genotypes
A Dominant form of Congenital Stationary Night Blindness (adCSNB) in a Large Chinese Family
Application of the Stepwise Focusing Method to Optimize the Cost-effectiveness of Genome-wide Association Studies with Limited Research Budgets for Genotyping and Phenotyping
Integrating Case-control and TDT Studies