Search Results 121-130 of 76308 for Genetic
Females with this genetic disorder have three X chromosomes instead of two. Symptoms can be mild or include developmental delays and learning disabilities.
... genetic mutation that caused him to develop frontotemporal dementia — a condition that greatly altered his personality and behavior. Attempting to piece the ...
The lab has assessed the association of the top GWAS variants and the apolipoprotein ε4 (APOE ε4) allele with memory, as well as progression to mild cognitive ...
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 ...
Sometimes, genetic testing finds a gene change that healthcare professionals aren't sure about. This is called a variant of unknown significance. A genetics ...
About this study. The purpose of the research is to identify mutations (defects in the genetic blueprint) that cause spontaneous coronary artery dissection ...
The genetic changes that cause familial hypercholesterolemia are present from birth, but symptoms may not appear until adulthood. There are two types of ...
Contact the Schaid Statistical Genetics and Genetic Epidemiology Lab at Mayo Clinic about methodology and software for genetic studies or about ...
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 ...
"We found that the patients who had one of these genetic mutations — especially if they were mutations in homologous recombination repair genes, including BRCA2 ...
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