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Preventing lives affected by hemophilia: A mixed methods study of the views of adults with hemophilia and their families toward genetic screening
BACKGROUND: Genomic sequencing technologies have made the possibility of population screening for whole panels of genetic disorders more feasible than ever before. As one of the most common single gene disorders affecting the UK population, hemophilia is an attractive candidate to include on such sc...
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| Publicat a: | Mol Genet Genomic Med |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6503017/ https://ncbi.nlm.nih.gov/pubmed/30838796 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.618 |
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