Loading...
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...
Na minha lista:
| Main Authors: | , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2012
|
| Fag: | |
| Online adgang: | 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 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|