Original language | English |
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Pages (from-to) | 793-795 |
Number of pages | 3 |
Journal | Journal of Intellectual Disability Research |
Volume | 57 |
Issue number | 9 |
DOIs | |
Publication status | Published - Sept 2013 |
Bibliographical note
Export Date: 23 March 2015CODEN: JIDRE
Correspondence Address: De Vries, P.J.; Division of Child and Adolescent Psychiatry, University of Cape Town, Cape Town, South Africa
References: Adnams, C.M., Perspectives of intellectual disability in South Africa: epidemiology, policy, services for children and adults (2010) Current Opinion in Psychiatry, 23, pp. 436-440; Christianson, A.L., Zwane, M.E., Manga, P., Rosen, E., Venter, A., Downs, D., Children with intellectual disability in rural South Africa: prevalence and associated disability (2002) Journal of Intellectual Disability Research, 46, pp. 179-186; Elsabbagh, M., Divan, G., Koh, Y., Kim, Y.S., Kauchali, S., Marcin, C., Global prevalence of autism and other pervasive developmental disorders (2012) Autism Research, 5, pp. 160-179; Kleintjes, S., Flisher, A.J., Fick, M., Railoun, A., Lund, C., Molteno, C., The prevalence of mental disorders among children, adolescents and adults in the western Cape, South Africa (2009) South African Psychiatry Review, 9, pp. 157-160; Martin, G.E., Ausderau, K.K., Raspa, M., Bishop, E., Mallya, U., Bailey Jr, D.B., Therapy service use among individuals with fragile X syndrome: findings from a U.S. parent survey (2013) Journal of Intellectual Disability Research, 57, pp. 825-837; Mazaheri, M.M., Rae-Seebach, R.D., Preston, H.E., Schmidt, M., Kountz-Edwards, S., Field, N., The impact of Prader-Willi syndrome on the family's quality of life and caregiving, and the unaffected siblings' psychosocial adjustment (2013) Journal of Intellectual Disability Research, 57, pp. 867-879; McCary, L.M., Roberts, J.E., Early identification of autism in fragile X syndrome: a review (2013) Journal of Intellectual Disability Research, 57, pp. 838-849
Keywords
- Adolescent
- Africa
- Behavior
- Biomedical Research
- Child
- Developmental Disabilities
- Genetic Diseases, Inborn
- Humans
- Intellectual Disability
- Phenotype