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Year | Number of Results |
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2018 | 2 |
2019 | 1 |
2024 | 0 |
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Updated recommendation for the benign stand-alone ACMG/AMP criterion.
Hum Mutat. 2018 Nov;39(11):1525-1530. doi: 10.1002/humu.23642.
Hum Mutat. 2018.
PMID: 30311383
Free PMC article.
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Hart MR, Biesecker BB, Blout CL, Christensen KD, Amendola LM, Bergstrom KL, Biswas S, Bowling KM, Brothers KB, Conlin LK, Cooper GM, Dulik MC, East KM, Everett JN, Finnila CR, Ghazani AA, Gilmore MJ, Goddard KAB, Jarvik GP, Johnston JJ, Kauffman TL, Kelley WV, Krier JB, Lewis KL, McGuire AL, McMullen C, Ou J, Plon SE, Rehm HL, Richards CS, Romasko EJ, Miren Sagardia A, Spinner NB, Thompson ML, Turbitt E, Vassy JL, Wilfond BS, Veenstra DL, Berg JS, Green RC, Biesecker LG, Hindorff LA.
Hart MR, et al.
Genet Med. 2019 May;21(5):1100-1110. doi: 10.1038/s41436-018-0308-x. Epub 2018 Oct 5.
Genet Med. 2019.
PMID: 30287922
Free PMC article.
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