Large and rare duplications and deletions in a chromosome region known as 22q11.2 , which involves genes that regulate cardiac development, are linked to nonsyndromic bicuspid aortic valve disease.

Scientists found that healthy women can carry genetic changes in their breast cells that are thought to be characteristic of ...

The gene DYRK1A could be a potential therapeutic target to treat ‘glue ear’ in people with Down syndrome, according to a new study.

The genetic cause for the most common type of hearing loss in children with Down syndrome has been identified in mice by ...

Large and rare duplications and deletions in a chromosome region known as 22q11.2 , which involves genes that regulate ...

The first step in the development of such an assay was provided by the isolation and characterization of a set of 41 cosmid, P1 and PAC clones specific for all human subtelomeric chromosome ...

The genetic cause for the most common type of hearing loss in children with Down syndrome has been identified in mice by researchers at UCL, the ...

The iPhone 16 Pro Mx comes with 6.9-icnh OLED display with 120Hz refresh rate and Apple's A18 Pro processor. Specs also include Triple camera setup on the back and better battery life than the ...

In many organisms, aging is a clear risk factor for increased rates of chromosome mis-segregation, the main source of aneuploidy. Here, we report that old yeast mother c ...