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

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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
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  Data: Increased frequency of CHEK2 germline pathogenic variants among individuals with dermatofibrosarcoma protuberans.
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  Data: <searchLink fieldCode="AU" term="%22Sargen+MR%22">Sargen MR</searchLink>; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD.<br /><searchLink fieldCode="AU" term="%22Kim+J%22">Kim J</searchLink>; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD.<br /><searchLink fieldCode="AU" term="%22Haley+JS%22">Haley JS</searchLink>; Department of Genomic Health, Geisinger Clinic, Geisinger Health System, Danville, PA.<br /><searchLink fieldCode="AU" term="%22Barker+HP%22">Barker HP</searchLink>; Garvan Institute of Medical Research, Sydney, NSW, Australia.<br /><searchLink fieldCode="AU" term="%22Mundra+PA%22">Mundra PA</searchLink>; Garvan Institute of Medical Research, Sydney, NSW, Australia.; St Vincent's Clinical School, University of New South Wales, Sydney, NSW, Australia.<br /><searchLink fieldCode="AU" term="%22Ballinger+ML%22">Ballinger ML</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Thomas+DM%22">Thomas DM</searchLink>; Garvan Institute of Medical Research, Sydney, NSW, Australia.; Centre for Molecular Oncology, University of New South Wales, Sydney, NSW, Australia.<br /><searchLink fieldCode="AU" term="%22Carey+DJ%22">Carey DJ</searchLink>; Department of Genomic Health, Geisinger Clinic, Geisinger Health System, Danville, PA.<br /><searchLink fieldCode="AU" term="%22Goldstein+AM%22">Goldstein AM</searchLink>; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD.<br /><searchLink fieldCode="AU" term="%22Stewart+DR%22">Stewart DR</searchLink>; Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Rockville, MD.
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  Data: <searchLink fieldCode="JN" term="%229918734281906676%22">Genetics in medicine open</searchLink> [Genet Med Open] 2024 Sep 28; Vol. 2, pp. 101895. <i>Date of Electronic Publication: </i>2024 Sep 28 (<i>Print Publication: </i>2024).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier+Inc%22">Elsevier Inc </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9918734281906676 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>2949-7744 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2229497744%22">29497744 </searchLink><i>NLM ISO Abbreviation: </i>Genet Med Open <i>Subsets: </i>PubMed not MEDLINE
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              Text: 2024 Sep 28
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