Genetics

Genomic sequencing enhances findings of hearing loss in NICU

Expanded genomic sequencing may be an effective adjunct hearing screening to detect hearing loss among patients in the neonatal intensive care unit (NICU), according to a study published online July 11 in JAMA Network Open.

Genetics

New genes with mutations for developmental disorders identified

The causes of intelligence impairment or epilepsy remain unexplained in more than 50% of cases. Together with international colleagues, researchers at Leipzig University Hospital have discovered two genes with mutations that ...

page 11 from 40