Copy number variation (CNV) has recently been identified as a major cause of structural variation in the genome, involving both duplications ... 606-16 (2005) Fellermann, K. et al. A chromosome ...
as well as missing copies of chromosome 16. The most frequent chromosome changes in these healthy women were extra copies in chromosome 1, and losses of chromosomes 16, 10 and 22, which scientists ...
Researchers have identified a key gene that drives susceptibility to ‘glue ear’ in people with Down syndrome, paving the way for future targeted therapies.