Congenital, Hereditary, and Neonatal Diseases and Abnormalities: News and Research on Congenital Abnormalities

MeSH tree: C16.131

Rare MGRN1 gene variant tied to fetal heart malformations

The Human Genetics Research Group of the University of Tartu Faculty of Medicine has identified a gene whose defect may cause congenital heart malformations in the fetus. The MGRN1 gene has not previously been associated ...

Scalable sensors lower the cost of studying genetic disorders

Researchers have demonstrated a new class of low-cost, scalable sensors that can be used to monitor electrical activity in human cerebral organoids. Because electrical signals are key to understanding brain function, this ...

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