Increased frequency of CHEK2 germline pathogenic variants among individuals with dermatofibrosarcoma protuberans.

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Bibliographic Details
Title: Increased frequency of CHEK2 germline pathogenic variants among individuals with dermatofibrosarcoma protuberans.
Authors: Sargen MR; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD., Kim J; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD., Haley JS; Department of Genomic Health, Geisinger Clinic, Geisinger Health System, Danville, PA., Barker HP; Garvan Institute of Medical Research, Sydney, NSW, Australia., Mundra PA; Garvan Institute of Medical Research, Sydney, NSW, Australia.; St Vincent's Clinical School, University of New South Wales, Sydney, NSW, Australia., Ballinger ML; Garvan Institute of Medical Research, Sydney, NSW, Australia.; St Vincent's Clinical School, University of New South Wales, Sydney, NSW, Australia.; School of Biomedical Sciences, University of New South Wales, Sydney, NSW, Australia., Thomas DM; Garvan Institute of Medical Research, Sydney, NSW, Australia.; Centre for Molecular Oncology, University of New South Wales, Sydney, NSW, Australia., Carey DJ; Department of Genomic Health, Geisinger Clinic, Geisinger Health System, Danville, PA., Goldstein AM; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD., Stewart DR; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD.
Source: Genetics in medicine open [Genet Med Open] 2024 Sep 28; Vol. 2, pp. 101895. Date of Electronic Publication: 2024 Sep 28 (Print Publication: 2024).
Publication Type: Journal Article
Journal Info: Publisher: Elsevier Inc Country of Publication: United States NLM ID: 9918734281906676 Publication Model: eCollection Cited Medium: Internet ISSN: 2949-7744 (Electronic) Linking ISSN: 29497744 NLM ISO Abbreviation: Genet Med Open Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2949-7744
DOI:10.1016/j.gimo.2024.101895