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SATB2‐associated syndrome: Mechanisms, phenotype, and practical recommendations
The SATB2‐associated syndrome is a recently described syndrome characterized by developmental delay/intellectual disability with absent or limited speech development, craniofacial abnormalities, behavioral problems, dysmorphic features, and palatal and dental abnormalities. Alterations of the SATB2...
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| 出版年: | Am J Med Genet A |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5297989/ https://ncbi.nlm.nih.gov/pubmed/27774744 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.38022 |
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