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IGF1R Variants Associated with Isolated Single Suture Craniosynostosis
The genetic contribution to the pathogenesis of isolated single suture craniosynostosis is poorly understood. The role of mutations in genes known to be associated with syndromic synostosis appears to be limited. We present our findings of a candidate gene resequencing approach to identify rare vari...
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| 主要な著者: | , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2011
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3059230/ https://ncbi.nlm.nih.gov/pubmed/21204214 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.33781 |
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