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Evaluating rare coding variants as contributing causes to nonsyndromic cleft lip and palate
Rare coding variants are a current focus in studies of complex disease. Previously, at least 68 rare coding variants were reported from candidate gene sequencing studies in nonsyndromic cleft lip and palate (NSCL/P), a common birth defect. Advances in sequencing technology have now resulted in thous...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3788862/ https://ncbi.nlm.nih.gov/pubmed/22978696 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.12018 |
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