Search Results 71-80 of 52184 for Genetic
Genotyping allows researchers to study genetic variations and mutations that may contribute to migraines. A genomic library is a collection of biological ...
A new study found that the presence of a specific genetic mutation strongly indicates a higher risk of cancer spread and worse survival rates for patients ...
"The gene can now be included in genetic testing for people suspected of having a neurodevelopmental disorder, which may end the diagnostic odyssey these people ...
Patients with certain established malignancies also should be further assessed for hereditary syndromes. Two other patient profiles suggest a need for genetic ...
This genetic condition stops typical development in parts of the body. It may include unusual facial features, short height, heart problems or other issues.
The purpose of this study is to genomically characterize pectus excavatum for the purpose of identifying candidate genes that may be causal in families with ...
Long-term objective. By studying the genes of individuals with HLHS and their family members, researchers hope to better understand the genetic underpinnings of ...
They might consider genetic testing and family planning options. If an at-risk parent is considering genetic testing, it can be helpful to meet with a genetic ...
Researchers discover that when meningiomas — the most common type of brain tumor — shows activity in the TERT gene, it tends to recur more quickly.
Finding which gene change caused Prader-Willi syndrome can help with genetic counseling. Risk factors. A child with an error in one or more genes in chromosome ...
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