References
- Niebuhr E. The cri du chat syndrome. Human Genetics 1978; 42: 143–156
- Cornish K, Bramble D. Cri-du-chat syndrome: Genotype-phenotype correlations and recommendations for clinical management. Developmental Medicine & Child Neurology 2002; 44: 494–497
- Higurashi M, Oda M, Iijma K, Iijma S, Takeshita T, Watanabe N, Yoneyama K. Livebirth prevalence and follow-up of malformation syndromes in 27,427 newborns. Brain Development 1990; 12: 770–773
- Ohr PS. Cri-du-Chat syndrome. Health-related disorders in children and adolescents: A guidebook for understanding and educating, L Phelps. American Psychological Association, Washington, DC 1998; 192–196
- Lejeune J, Lafourcade J, Berger R, Vialatte J, Boeswillwald M, Seringe P, Turpin R. Trois cas de la deletion partielle du bras court du chromosome 5. Comptes Rendus Hebdomadaire des Seances de l’ Academie des Sciences: D. Sciences Naturelles 1963; 257: 3098–3102
- Cornish KM, Cross G, Green A, Willatt L, Bradshaw JM. A neuropsychological-genetic profile of atypical cri du chat syndrome: Implications for prognosis. Journal of Medical Genetics 1999; 36: 567–570
- Beukelman DR, Mirenda P. Augmentative and alternative communication: Supporting children and adults with complex communication needs, 3rd. Paul H. Brookes, Baltimore 2005
- Snell ME, Brown F. Instruction of students with severe disabilities, 6th. Person, Upper Saddle River, NJ 2006
- Duker PC, van Driel S, van de Bercken J. Communication profiles of individuals with Down's syndrome, Angelman syndrome and pervasive developmental disorder. Journal of Intellectual Disability Research 2002; 46: 35–40