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Whole-exome sequencing for finding de novo mutations in sporadic mental retardation
Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation.
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2010
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| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3046476/ https://ncbi.nlm.nih.gov/pubmed/21172032 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2010-11-12-144 |
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