New chromosome-level evidence suggests Medicago evolution followed a more complex, and surprising path, than previously ...

Researchers at City of Hope, a cancer research and treatment organization, and the University of California, Berkeley, have ...

In a prospective validation study, researchers at The University of Texas MD Anderson Cancer Center have demonstrated that a ...

For years, two siblings with the distinctive facial features of Treacher Collins syndrome had no genetic explanation for ...

Congenital heart disease (CHD) is the most common birth defect and a leading cause of infant mortality. CHD often has a genetic cause, and recent studies demonstrate the utility of genetic testing. In ...

Daniel Combs, MD, is an Assistant Professor of Pediatrics and Medicine at the University of Arizona. Clinical signs raise suspicion for Prader-Willi syndrome (PWS), but genetic testing confirms it.

We report a family with X-linked ichthyosis (XLI), in which the non-invasive prenatal testing (NIPT) results from the pregnant woman revealed a deletion of approximately 2 Mb at Xp22.31, confirmed by ...

SAN DIEGO, Feb. 26, 2026 (GLOBE NEWSWIRE) -- Bionano Genomics, Inc. (Nasdaq: BNGO) today announced highlights from Day 3 of Bionano Symposium 2026, entitled OGM Making its Mark in Constitutional ...

HOUSTON, TX, UNITED STATES, February 24, 2026 /EINPresswire.com/ — FamilyTreeDNA, the company that pioneered the genetic genealogy industry, today announced a ...

SITUS inversus totalis diagnosed prenatally plus DNAH11 variants highlights why imaging and genetic testing guide counseling today. Situs inversus totalis (SIT) is a rare congenital laterality ...