Učitavanje...
Using whole exome sequencing to identify candidate genes with rare variants in nonsyndromic cleft lip and palate
INTRODUCTION: Studies suggest that nonsyndromic cleft lip and palate (NSCLP) is polygenic with variable penetrance, presenting a challenge in identifying all causal genetic variants. Despite relatively high prevalence of NSCLP among Amerindian populations, no large whole exome sequencing (WES) studi...
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| Izdano u: | Genet Epidemiol |
|---|---|
| Glavni autori: | , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2016
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4985012/ https://ncbi.nlm.nih.gov/pubmed/27229527 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.21972 |
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