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| Autism | 1 |
| Clinical Diagnosis | 1 |
| Diseases | 1 |
| Down Syndrome | 1 |
| Genetics | 1 |
| Interdisciplinary Approach | 1 |
| Symptoms (Individual… | 1 |
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| Journal of Autism and… | 1 |
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| Baumann, Clarisse | 1 |
| Burglen, Lydie | 1 |
| Cohen, David | 1 |
| Excoffier, Elsa | 1 |
| Heron, Delphine | 1 |
| Lazar, Gabriela | 1 |
| Mazet, Philippe | 1 |
| Pichard, Nadege | 1 |
| Pinquier, Clement | 1 |
| Tordjman, Sylvie | 1 |
| Verloes, Alian | 1 |
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| Journal Articles | 1 |
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Direct linkCohen, David; Pichard, Nadege; Tordjman, Sylvie; Baumann, Clarisse; Burglen, Lydie; Excoffier, Elsa; Lazar, Gabriela; Mazet, Philippe; Pinquier, Clement; Verloes, Alian; Heron, Delphine – Journal of Autism and Developmental Disorders, 2005
Autism is a heterogeneous disorder that can reveal a specific genetic disease. This paper describes several genetic diseases consistently associated with autism (fragile X, tuberous sclerosis, Angelman syndrome, duplication of 15q11-q13, Down syndrome, San Filippo syndrome, MECP2 related disorders, phenylketonuria, Smith-Magenis syndrome, 22q13…
Descriptors: Down Syndrome, Genetics, Autism, Diseases
