1p36 Deletion Syndrome (1p36DS) is a genetic condition caused by the deletion of a portion of the short arm of chromosome 1. It is one of the most common terminal deletion syndromes, with an ...

T he chromosomal disorder 22q11.2 deletion syndrome (22q) has emerged as one of the strongest risks for schizophrenia. Scientists at St. Jude Children's Research Hospital identified malformed ...

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

DiGeorge syndrome, a 22q11.2 deletion syndrome, is caused when a small portion of chromosome 22 is missing. The condition can occur in individuals born from a parent with the dominant contiguous ...