Carregant...
Whole Exome Association of Rare Deletions in Multiplex Oral Cleft Families
By sequencing the exomes of distantly related individuals in multiplex families, rare mutational and structural changes to coding DNA can be characterized and their relationship to disease risk can be assessed. Recently, several rare single nucleotide variants (SNVs) were associated with an increase...
Guardat en:
| Publicat a: | Genet Epidemiol |
|---|---|
| Autors principals: | , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2016
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5154821/ https://ncbi.nlm.nih.gov/pubmed/27910131 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.22010 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|