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Information exchange between patients with Lynch syndrome and their genetic and non-genetic health professionals: whose responsibility?
Individuals at high risk for Lynch syndrome (LS) should be offered genetic counselling, since preventive options are available. However, uptake of genetic services and follow-up care are currently suboptimal, possibly caused by inadequate exchange of information. Therefore, this qualitative study ai...
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| Publicado en: | J Community Genet |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Springer Berlin Heidelberg
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6435774/ https://ncbi.nlm.nih.gov/pubmed/30209752 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12687-018-0381-5 |
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