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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Veröffentlicht in:J Community Genet
Hauptverfasser: Douma, Kirsten F. L., Bleeker, Fonnet E., Medendorp, Niki M., Croes, Emmelyn A. J., Smets, Ellen M. A.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Springer Berlin Heidelberg 2018
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Original Paper
Online Zugang: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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