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196 results

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Efforts Toward Consensus Variant Interpretation by Commercial Laboratories.
Dolinsky JS, Hruska KS, Pesaran T, Richardson ME, Klein RT, Solomon BD, Gau CL. Dolinsky JS, et al. Among authors: solomon bd. J Clin Oncol. 2017 Apr 10;35(11):1261-1262. doi: 10.1200/JCO.2016.71.2505. Epub 2017 Jan 30. J Clin Oncol. 2017. PMID: 28135139 No abstract available.
Response to ten Broeke et al.
Roberts ME, Zeinomar N, Solomon BD, Terry MB, Chung WK. Roberts ME, et al. Among authors: solomon bd. Genet Med. 2019 Jan;21(1):258-259. doi: 10.1038/s41436-018-0031-7. Epub 2018 May 24. Genet Med. 2019. PMID: 29795440 Free PMC article. No abstract available.
Utility of Expedited Hereditary Cancer Testing in the Surgical Management of Patients with a New Breast Cancer Diagnosis.
Theobald KA, Susswein LR, Marshall ML, Roberts ME, Mester JL, Speyer D, Williams RNW, Knapke SC, Solomon SR, Murphy PD, Klein RT, Hruska KS, Solomon BD. Theobald KA, et al. Among authors: solomon sr, solomon bd. Ann Surg Oncol. 2018 Nov;25(12):3556-3562. doi: 10.1245/s10434-018-6581-8. Epub 2018 Aug 30. Ann Surg Oncol. 2018. PMID: 30167906
Germline pathogenic variants identified in women with ovarian tumors.
Carter NJ, Marshall ML, Susswein LR, Zorn KK, Hiraki S, Arvai KJ, Torene RI, McGill AK, Yackowski L, Murphy PD, Xu Z, Solomon BD, Klein RT, Hruska KS. Carter NJ, et al. Among authors: solomon bd. Gynecol Oncol. 2018 Dec;151(3):481-488. doi: 10.1016/j.ygyno.2018.09.030. Epub 2018 Oct 12. Gynecol Oncol. 2018. PMID: 30322717
Response to Evans et al.
Roberts ME, Zeinomar N, Solomon BD, Terry MB, Chung WK. Roberts ME, et al. Among authors: solomon bd. Genet Med. 2019 Aug;21(8):1880-1881. doi: 10.1038/s41436-018-0400-2. Epub 2018 Dec 19. Genet Med. 2019. PMID: 30563985 Free article. No abstract available.
Response to Wang et al.
Roberts ME, Zeinomar N, Solomon BD, Terry MB, Chung WK. Roberts ME, et al. Among authors: solomon bd. Genet Med. 2019 Sep;21(9):2158. doi: 10.1038/s41436-019-0469-2. Epub 2019 Mar 1. Genet Med. 2019. PMID: 30824819 Free article. No abstract available.
Phenotypic diversity of patients diagnosed with VACTERL association.
Husain M, Dutra-Clarke M, Lemieux B, Wencel M, Solomon BD, Kimonis V. Husain M, et al. Among authors: solomon bd. Am J Med Genet A. 2018 Sep;176(9):1830-1837. doi: 10.1002/ajmg.a.40363. Epub 2018 Aug 27. Am J Med Genet A. 2018. PMID: 30152190
196 results