Search Results 251-260 of 48979 for Genetic
This study is being done to identify underlying genetic defects in individuals from families who are at-risk of a possible cardiac channelopathy (abnormal ...
His rare genetic disorder enlarged his tongue and head, and he had weakened muscle tone, brittle bones, sleep apnea, poor eyesight and persistent infections in ...
For the past decade, heart failure in RBM20 cardiomyopathy was attributed to abnormalities in the splicing of genes for proteins that help the heart contract.
... genetic material biobank to better characterize the symptoms and unknown genetic causes of Angelman syndrome. Participation eligibility. Participant ...
The placenta contains the same genetic material as the baby. The chorionic villus cells can be sent to the genetics lab for chromosome studies. This is ...
This basic idea is key to understanding how genes are expressed and how to overcome genetic defects that cause disease. ... genetic defect in sickle-cell disease.
Risk factors for congenital heart disease include: Genetics. Congenital heart disease appears to run in families, which means it is inherited. Changes in genes ...
Meagher, whose academic interests include the ethics of emerging genetic technologies and their health care implications. "Medical professionals should expect ...
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.
Mayo Clinic does not endorse companies or products. Advertising revenue supports our not-for-profit mission.
Check out these best-sellers and special offers on books and newsletters from Mayo Clinic Press.