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Uptake of genetic testing by the children of Lynch syndrome variant carriers across three generations
Many Lynch syndrome (LS) carriers remain unidentified, thus missing early cancer detection and prevention opportunities. Tested probands should inform their relatives about cancer risk and options for genetic counselling and predictive gene testing, but many fail to undergo testing. To assess predic...
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| Опубликовано в: : | Eur J Hum Genet |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Nature Publishing Group
2017
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5643966/ https://ncbi.nlm.nih.gov/pubmed/28832568 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2017.132 |
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