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Exploring the 7p22.1 Chromosome as a Candidate Region for Autism
A high incidence of de novo chromosomal aberrations in a population of persons with autism suggests a causal relationship between certain chromosomal aberrations and the occurrence of autism. A previous study on a Tunisian boy carrying a t(7;16) translocation identified the 7p22.1 as a positional ca...
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| Hoofdauteurs: | , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Hindawi Publishing Corporation
2010
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2856063/ https://ncbi.nlm.nih.gov/pubmed/20414355 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2010/423894 |
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