Subject Areas on Research
- Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.
- Copy number variation is associated with gene expression change in archaea.
- Further clinical and molecular delineation of the 15q24 microdeletion syndrome.
- High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacy.