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...

Descripción completa

Detalles Bibliográficos
Autores principales: Douma, Kirsten F. L., Bleeker, Fonnet E., Medendorp, Niki M., Croes, Emmelyn A. J., Smets, Ellen M. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435774/
https://www.ncbi.nlm.nih.gov/pubmed/30209752
http://dx.doi.org/10.1007/s12687-018-0381-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435774/
https://www.ncbi.nlm.nih.gov/pubmed/30209752
http://dx.doi.org/10.1007/s12687-018-0381-5

Ejemplares similares