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Page 1
Response to Stern.
Hanson H, Astiazaran-Symonds E, Amendola LM, Balmaña J, Foulkes WD, James P, Klugman S, Ngeow J, Schmutzler R, Voian N, Wick MJ, Pal T, Tischkowitz M, Stewart DR. Hanson H, et al. Among authors: klugman s. Genet Med. 2024 Feb;26(2):101030. doi: 10.1016/j.gim.2023.101030. Epub 2023 Dec 29. Genet Med. 2024. PMID: 38156990 No abstract available.
Management of individuals with germline pathogenic/likely pathogenic variants in CHEK2: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Hanson H, Astiazaran-Symonds E, Amendola LM, Balmaña J, Foulkes WD, James P, Klugman S, Ngeow J, Schmutzler R, Voian N, Wick MJ, Pal T, Tischkowitz M, Stewart DR; ACMG Professional Practices and Guidelines Committee. Electronic address: documents@acmg.net. Hanson H, et al. Among authors: klugman s. Genet Med. 2023 Oct;25(10):100870. doi: 10.1016/j.gim.2023.100870. Epub 2023 Jul 25. Genet Med. 2023. PMID: 37490054
Points to consider: is there evidence to support BRCA1/2 and other inherited breast cancer genetic testing for all breast cancer patients? A statement of the American College of Medical Genetics and Genomics (ACMG).
Pal T, Agnese D, Daly M, La Spada A, Litton J, Wick M, Klugman S, Esplin ED, Jarvik GP; Professional Practice and Guidelines Committee. Pal T, et al. Among authors: klugman s. Genet Med. 2020 Apr;22(4):681-685. doi: 10.1038/s41436-019-0712-x. Epub 2019 Dec 13. Genet Med. 2020. PMID: 31831881 Free article. No abstract available.
Response to Prensky and Persson.
Dungan JS, Klugman S. Dungan JS, et al. Among authors: klugman s. Genet Med. 2023 Sep;25(9):100873. doi: 10.1016/j.gim.2023.100873. Epub 2023 Jun 2. Genet Med. 2023. PMID: 37266582 No abstract available.
Response to Righetti et al.
Dungan JS, Aarabi M, Klugman S, Gregg AR. Dungan JS, et al. Among authors: klugman s. Genet Med. 2022 May;24(5):1162-1163. doi: 10.1016/j.gim.2021.12.017. Epub 2022 Feb 25. Genet Med. 2022. PMID: 35221206 Free article. No abstract available.
Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).
Dungan JS, Klugman S, Darilek S, Malinowski J, Akkari YMN, Monaghan KG, Erwin A, Best RG; ACMG Board of Directors. Electronic address: documents@acmg.net. Dungan JS, et al. Among authors: klugman s. Genet Med. 2023 Feb;25(2):100336. doi: 10.1016/j.gim.2022.11.004. Epub 2022 Dec 16. Genet Med. 2023. PMID: 36524989 Free article.
Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).
Dungan JS, Klugman S, Darilek S, Malinowski J, Akkari YMN, Monaghan KG, Erwin A, Best RG; ACMG Board of Directors. Dungan JS, et al. Among authors: klugman s. Genet Med. 2023 Aug;25(8):100874. doi: 10.1016/j.gim.2023.100874. Epub 2023 Jun 27. Genet Med. 2023. PMID: 37378664 No abstract available.
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