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The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British Columbia.
Elliott AM, du Souich C, Adam S, Dragojlovic N, van Karnebeek C, Nelson TN, Lehman A; CAUSES Study; Lynd LD, Friedman JM. Elliott AM, et al. Among authors: lynd ld. Mol Genet Genomic Med. 2018 May 30;6(4):592-600. doi: 10.1002/mgg3.410. Online ahead of print. Mol Genet Genomic Med. 2018. PMID: 29851296 Free PMC article.
Integration of genetic counsellors in genomic testing triage: Outcomes of a genomic consultation service in British Columbia, Canada.
Cook CB, Dragojlovic N, Siemens A, Adam S, du Souich C, van Karnebeek C, Lehman A, Nelson TN, Friedman J; CAUSES Study; GenCOUNSEL Study; Lynd LD, Elliott AM. Cook CB, et al. Among authors: lynd ld. Eur J Med Genet. 2021 Jul;64(7):104024. doi: 10.1016/j.ejmg.2020.104024. Epub 2020 Aug 14. Eur J Med Genet. 2021. PMID: 32798762
Toward the diagnosis of rare childhood genetic diseases: what do parents value most?
Pollard S, Weymann D, Dunne J, Mayanloo F, Buckell J, Buchanan J, Wordsworth S, Friedman JM, Stockler-Ipsiroglu S, Dragojlovic N, Elliott AM, Harrison M, Lynd LD, Regier DA. Pollard S, et al. Among authors: lynd ld. Eur J Hum Genet. 2021 Oct;29(10):1491-1501. doi: 10.1038/s41431-021-00882-1. Epub 2021 Apr 26. Eur J Hum Genet. 2021. PMID: 33903739 Free PMC article.
202 results