Williams syndrome, also called Williams-Beuren syndrome, is a rare genetic disorder. ... Scientists found that a deletion in chromosome 7 causes this condition.

Williams syndrome is a developmental disorder that can affect the body in a variety of ways, from influencing intellectual development and cardiovascular function to altering personality traits and ...

People with Williams Syndrome treat strangers as their new best friends. Now the condition is revealing clues to our evolutionary past – and what makes us human.

Williams Syndrome is a genetic condition that affects one in 10,000 people worldwide. Dr Waggoner says it stems from a chromosome abnormality. “This is a picture of chromosome 7.

A rare genetic disorder, Williams Syndrome, affects around 1 in 7,500 to 10,000 people worldwide. It is caused by the deletion of a small segment of chromosome 7, which contains 25–27 genes.

Williams syndrome, which affects 30,000 people in the U.S., ... about 26 to 28 missing genes on chromosome 7. There are some serious symptoms, like intellectual disability, ...

Williams syndrome is a genetic condition caused by a deletion of genetic material in a region of chromosome 7, which can result in unique physical features and cardiovascular abnormalities.

People with Williams Syndrome treat strangers as their new best friends. Now the condition is giving clues to our evolutionary past – and what makes us human. Imagine walking down the street and ...