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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...

詳細記述

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書誌詳細
主要な著者: Laje, Gonzalo, Morse, Rebecca, Richter, William, Ball, Jonathan, Pao, Maryland, Smith, Ann C.M.
フォーマット: Artigo
言語:Inglês
出版事項: 2010
主題:
オンライン・アクセス: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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