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Autism Spectrum Features in Smith-Magenis Syndrome
Smith-Magenis syndrome (SMS; OMIM 182290) is a neurodevelopmental disorder characterized by a well-defined pattern of anomalies. The majority of cases are due to a common deletion in chromosome 17p11.2 that includes the RAI1 gene. In children with SMS, autistic-like behaviors and symptoms start to e...
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| Huvudupphovsmän: | , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2010
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2967410/ https://ncbi.nlm.nih.gov/pubmed/20981775 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.c.30275 |
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