Approaches to Handling Incomplete Data in Family-based Association Testing
Epistatic Interactions between Genomic Regions Containing the COL1A1 Gene and Genes Regulating Osteoclast Differentiation may Influence Femoral Neck Bone Mineral Density
Interrelationship and Familiality of Dyslexia Related Quantitative Measures
Polymorphisms in the Angiotensin Converting Enzyme Gene and Growth in the First Year of Life
Molecular Epidemiology of Phenylalanine Hydroxylase Deficiency in Southern Italy
Spectrum of Mutations in the CFTR Gene in Cystic Fibrosis Patients of Spanish Ancestry
The Fate of 12 Recessive Mutations in A Single Village
Unbiased Interpretation of Haplotypes at Duplicated Microsatellites
A Two-Stage Approach to the Correction of Ascertainment Bias in Complex Genetic Studies Involving Variance Components
Mixed-effects Logistic Approach for Association Following Linkage Scan for Complex Disorders
Analysis of Case-Only Studies Accounting for Genotyping Error
The Effects of SNP Genotyping Errors on the Power of The Cochran-Armitage Linear Trend Test for Case/Control Association Studies
Computing power in case-control association studies through the use of quadratic approximations
Localization of a Novel Autosomal Recessive Non-syndromic Hearing Impairment Locus DFNB63 to Chromosome 11q13.3-q13.4
The Art of Reading Sequence Electropherograms
The Art of Reading Sequence Electropherograms
Editorial Note