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Autism and intellectual disability in a patient with two microdeletions in 6q16: a contiguous gene deletion syndrome?
BACKGROUND: Copy number variations play a significant role in the aetiology of developmental disabilities including non-syndromic intellectual disability and autism. CASE PRESENTATION: We describe a 19-year old patient with intellectual disability and autism for whom chromosomal microarray (CMA) ana...
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| Publicado no: | Mol Cytogenet |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5135825/ https://ncbi.nlm.nih.gov/pubmed/27980676 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-016-0299-8 |
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