Discover the facts about CLOVES syndrome—an extremely rare genetic disorder with complex symptoms and challenging diagnosis.

Baby with 1 Dad, 2 Mums brings major breakthrough in hereditary disease prevention and infertility treatment, doctors shed ...

An international research team has identified a new protein that specifically transports enzymes into peroxisomes. Its mode ...

Th<span id="cke_bm_479S" style="display:no is study aimed to bridge that gap by conducting genetic analysis on a cohort of ...

Molecular testing in dermatology involves decisions about who gets tested, how to test and interpret results, and where to go ...

Dear reader, Thursday is National Mutt Day and for dog owners it is a day to celebrate everything your BFF is. Unless you ...

A global study has identified the DNA markers for stuttering, providing a genetic link that will pave the way for clinicians ...

The Department for Work and Pensions (DWP) has fleshed out eligibily for a key benefit worth £110 per week - and dozens of ...

A study projects a sharp rise in uterine cancers over the next two decades, with even greater increases in Black women.

Kedrion Biopharma receives US FDA orphan drug designation for Coagadex to treat acquired Factor X deficiency: Fort Lee, New Jersey Thursday, July 31, 2025, 15:00 Hrs [IST] Kedrion ...

A global study has identified the DNA markers for stuttering, providing a genetic link that will pave the way for clinicians ...