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16p11.2 microdeletion syndrome: a case report
BACKGROUND: The recurrent ∼ 600 kb 16p11.2 microdeletion is among the most commonly known genetic etiologies of autism spectrum disorder, overweightness, and related neurodevelopmental disorders. CASE PRESENTATION: Our patient is a 2-year-old white girl from the first pregnancy of a non-consanguineo...
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| 出版年: | J Med Case Rep |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5881179/ https://ncbi.nlm.nih.gov/pubmed/29609622 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-018-1587-1 |
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