Mice genetically engineered to mimic human DiGeorge syndrome provide clues to the genetic basis of this chromosomal deletion syndrome and question UFD1L as the sole candidate gene. You have full ...

Ella Gregorich, from Great Gonerby, was born with DiGeorge syndrome, which can cause heart problems and learning difficulties. The three-year-old receives overnight care from trained nurses ...

A microdeletion of chromosome 22q11.2 is found in most patients with velocardiofacial syndrome, DiGeorge syndrome, and conotruncal anomaly face syndrome, and in some patients with Cayler ...

The common symptoms may include: Occurs due to deletion of a small part of chromosome 22. The missing gene is known as 22q11.2. This deletion causes defects in several systems of the body.

Clayton County police have confirmed that a body found in unincorporated Clayton County Tuesday afternoon is that of an ...