Search Results 91-100 of 21479 for Genetic
Testing helps determine if a patient carries genetic variants in CYP2C19 that cause loss of its function. These variants interfere with the body's ability to ...
About this study. The purpose of this research is to develop a collection of known mutation carriers to analyze cancer risk and long-term clinical outcomes.
To date there are approximately 65 common genetic variants reproducibly associated with type 2 diabetes mellitus. The greatest risk is associated with ...
About this study. Common variable immunodeficiency (CVID) is a clinically, genetically and immunologically heterogeneous primary immunodeficiency disease ...
This rare genetic disorder affects the way the brain develops, causing a progressive inability to use muscles for eye and body movements and language.
Answer: As with many diseases, the causes of rheumatoid arthritis appear to be a combination of genetic and environmental factors. The genetic factors that ...
Our research team in the Atherosclerosis and Lipid Genomics Laboratory has used a wide range of tools to understand the genetic basis of atherosclerotic ...
Long-term objective. By studying the genes of individuals with HLHS and their family members, researchers hope to better understand the genetic underpinnings of ...
This genetic disorder is extremely rare and progressive. It causes children to age rapidly, beginning in their first two years of life.
Females with this genetic disorder have three X chromosomes instead of two. Symptoms can be mild or include developmental delays and learning disabilities.
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