Human molecular genetics

Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis.

Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis.

Abnormal CpG island methylation occurs during in vitro differentiation of human embryonic stem cells.

Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15.

Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15.

PAX4 gene variations predispose to ketosis-prone diabetes.

PAX4 gene variations predispose to ketosis-prone diabetes.

The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway.

The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway.

Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping.

Pages