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Family-Specific Variants and the Limits of Human Genetics
Every single nucleotide change compatible with life is present in the human population today. Understanding these rare human variants defines an extraordinary challenge for genetics and medicine. The new clinical practice of sequencing many genes for hereditary cancer risk has illustrated the utilit...
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| Publicado no: | Trends Mol Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6197474/ https://ncbi.nlm.nih.gov/pubmed/27742414 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.molmed.2016.09.007 |
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