Á lódáil...
Identification of rare variants from exome sequence in a large pedigree with autism
We carried out analyses with the goal of identifying rare variants in exome sequence data that contribute to disease risk for a complex trait. We analyzed a large, 47-member multigenerational pedigree with 11 cases of autism spectrum disorder, using genotypes from three technologies representing inc...
Na minha lista:
| Main Authors: | , , , , , , , , , |
|---|---|
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2013
|
| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3722055/ https://ncbi.nlm.nih.gov/pubmed/23594493 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000346560 |
| Clibeanna: |
Cuir Clib Leis
Gan Chlibeanna, Bí ar an gcéad duine leis an taifead seo a chlibeáil!
|