Mutational Spectrum of the C1 Inhibitor Gene in a Cohort of Italian Patients with Hereditary Angioedema: Description of Nine Novel Mutations
A DFNA5 Mutation Identified in Japanese Families with Autosomal Dominant Hereditary Hearing Loss
Recent Radiation within Y-chromosomal Haplogroup R-M269 Resulted in High Y-STR Haplotype Resemblance
Tumor Necrosis Factor and Interleukin-6 Gene Polymorphisms and Endometriosis Risk in Asians: A Systematic Review and Meta-Analysis
A Family-Based Robust Multivariate Association Test Using Maximum Statistic
Utilising Family-Based Designs for Detecting Rare Variant Disease Associations
Nonparametric Tests of Associations with Disease Based on U-Statistics