1. Beeser, S. L., Donnenfeld, A. E., Miller, R. C., et al. (1994). Prenatal diagnosis of the derivative chromosome 22 associated with cat eye syndrome by fluorescence in situ hybridization. Prenatal Diagnosis, 14, 1029–1034.
2. Ben-Shachar, S., Ou, Z., Shaw, C. A., et al. (2008). 22q11.2 distal deletion: A recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome. American Journal of Human Genetics, 82, 214–221.
3. Berends, M. J., Tan-Sindhunata, G., Leegte, B., et al. (2001). Phenotypic variability of cat-eye syndrome. Genetic Counseling, 12, 23–34.
4. Bofinger, M. K., & Soukup, S. W. (1977). Cat eye syndrome. Partial trisomy 22 due to translocation in the mother. American Journal of Diseases of Children, 131, 893–897.
5. Chen, C.-P., Ko, T.-M., Su, J.-W., et al. (2013). Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome. Gene, 527, 384–388.