Search Results 261-270 of 49089 for Genetic
Risk factors for congenital heart disease include: Genetics. Congenital heart disease appears to run in families, which means it is inherited. Changes in genes ...
The purpose of this study is to identify common genetic variants contributing to the risk of glioma. Evaluate gene-gene and gene-environmental interactions with ...
Two of the most common genes were discovered in three cases (KCNQ1 and KCNH2); and five of the cases exhibited SCN5A rare non-synonymous genetic variants.
Females with this genetic disorder have three X chromosomes instead of two. Symptoms can be mild or include developmental delays and learning disabilities.
The purpose of this study is to validate a precision genetic testing approach guided by machine learning (ML)-based models. Participation eligibility.
Genetic testing can reveal whether you have these changes in your HFE gene. If you inherit two altered genes, you may develop hemochromatosis. You also can pass ...
Web-based genetic education before receiving tumor profiling results and remote genetic counseling for patients with potential germline mutations may increase ...
The purpose of this study is to identify novel genetic variants associated with stent thrombosis. Participation eligibility. Participant eligibility includes ...
... genetic variations that can help predict which patients will respond well to each available therapy, especially newly developed biological agents. The ...
BRCA gene mutations: Cancer risk and genetic testing. National Cancer Institute. https://www.cancer.gov/about-cancer/causes-prevention/genetics/brca-fact-sheet.
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