Researchers led by UC Davis Health scientist Sanchita Bhatnagar have developed a promising gene therapy that could treat Rett ...

An international team of scientists has decoded some of the most stubborn, overlooked regions of the human genome using ...

Next Saturday, at the Brown County Fairgrounds, truck enthusiasts will be gathering for a special fundraiser for Cashton ...

Noah Quish, a little Limerick boy who has undergone 15 surgeries related to the scoliosis he was born with, has been ...

Zenith said: “We’re concerned with his specific deletion, which we know is called Burnside Butler Syndrome, and this is linked to Prada Willi Syndrome also affecting chromosome 15.

It results from the loss of function of the UBE3A gene located on the 15th chromosome, specifically the copy inherited from the mother.

Researchers at the Francis Crick Institute studying male mice engineered with different Y chromosome deletions have uncovered which genes on the mouse Y chromosome regulate the development of ...

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 ...

Abstract The loss of a single chromosome in a diploid organism halves the dosage of many genes and is usually accompanied by a substantial decrease in fitness. We asked whether this decrease simply ...

While the brains of children with AS are completely normal and anatomically correct, a genetic microdeletion on the 15th chromosome causes massive global delays, including debilitating seizures ...