Hereditary non-syndromic deafness has been associated with a point mutation in the mitochondrial 12S rRNA gene. We present data from deaf individuals in 12 nuclear families originating from a small ...

Association of genetic variations within the T-cell costimulatory LIGHT gene with outcome in stage II and III colon cancer. This is an ASCO Meeting Abstract from the 2019 ASCO Annual Meeting I. This ...

Researchers from Tokyo Medical and Dental University (TMDU) and Cincinnati Children’s Hospital Medical Center (CCHMC) find that a point mutation in the glucokinase regulatory protein gene protects ...

Predictive value for survival of a risk model of two serological markers, beta-2-microglobulin (B2M) and lactic dehydrogenase (LDH), in diffuse large cell lymphoma (DLCL) No significant financial ...

SNP genotyping is an exciting field. The completion of the human genome sequencing project has enabled SNP research to move forward. SNP genotyping allows for further characterization of the human ...