Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report

Last 30 days: 86 accesses
Last 365 days: 870 accesses
All time: 2883 accesses

Roland Haj, Kelly Jackson, Beth A Torchia, Lisa G Shaffer, Bassem A Bejjani^*, Gordon C Gowans and Michael E Ruff