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Testing reported associations of genetic risk factors for oral clefts in a large Irish study population
BACKGROUND: Suggestive, but not conclusive, studies implicate many genetic variants in oral cleft etiology. We used a large, ethnically homogenous study population to test whether reported associations between nonsyndromic oral clefts and 12 genes (CLPTM1, CRISPLD2, FGFR2, GABRB3, GLI2, IRF6, PTCH1,...
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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: |
2010
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3503531/ https://ncbi.nlm.nih.gov/pubmed/19937600 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.20639 |
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