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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2017 | 1 |
2018 | 2 |
2019 | 2 |
2020 | 1 |
2024 | 0 |
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The cost and diagnostic yield of exome sequencing for children with suspected genetic disorders: a benchmarking study.
Genet Med. 2018 Sep;20(9):1013-1021. doi: 10.1038/gim.2017.226. Epub 2018 Jan 4.
Genet Med. 2018.
PMID: 29300375
Free article.
Review.
Evaluating Canadians' Values for Drug Coverage Decision Making.
Rizzardo S, Bansback N, Dragojlovic N, Douglas C, Li KH, Mitton C, Marra C, Blanis L, Lynd LD.
Rizzardo S, et al.
Value Health. 2019 Mar;22(3):362-369. doi: 10.1016/j.jval.2018.08.008. Epub 2018 Nov 27.
Value Health. 2019.
PMID: 30832975
Free article.
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Engaging the Canadian public on reimbursement decision-making for drugs for rare diseases: a national online survey.
Polisena J, Burgess M, Mitton C, Lynd LD.
Polisena J, et al.
BMC Health Serv Res. 2017 May 26;17(1):372. doi: 10.1186/s12913-017-2310-4.
BMC Health Serv Res. 2017.
PMID: 28549479
Free PMC article.
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The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders.
Dragojlovic N, van Karnebeek CDM, Ghani A, Genereaux D, Kim E, Birch P; CAUSES Study; Elliott AM, Friedman JM, Lynd LD.
Dragojlovic N, et al.
Genet Med. 2020 Feb;22(2):292-300. doi: 10.1038/s41436-019-0635-6. Epub 2019 Aug 29.
Genet Med. 2020.
PMID: 31462755
Free article.
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