1. Online Mendelian Inheritance in Man, OMIM (TM). [cited 2010 Mar 22].McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University (Baltimore, MD) and National Centre for Biotechnology Information, National Library of Medicine (Bethesda, MD), 2000. http://www.ncbi.nlm.nih.gov/omim/
2. Molecular characterization of the marker chromosome associated with cat eye syndrome;Mears;Am J Hum Genet,1994
3. Phenotypic variability of cat-eye syndrome;Berends;Genet Couns,2001
4. The “cat eye syndrome”: dicentric small marker chromosome probably derived from a no.22 (tetrasomy 22pter to q11) associated with a characteristic phenotype. Report of 11 patients and delineation of the clinical picture;Schinzel;Hum Genet,1981
5. A common molecular basis for rearrangement disorders on chromosome 22q11;Edelman;Hum Mol Genet,1999