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The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families

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第一作者: Pinheiro,M.
作者: Pinheiro,M. [1] ; Pinto,C. [2] ; Peixoto,A. [3] ; Veiga,I. [4] ; Mesquita,B. [5] ; Henrique,R. [6] ; Lopes,P. [7] ; Sousa,O. [8] ; Fragoso,M. [9] ; Dias,L. [10] ; Baptista,M. [11] ; Marinho,C. [12] ; Mangold,E. [13] ; Vaccaro,C. ; Evans,D. ; Farrington,S. ; Dunlop,M. ; Teixeira,M.
作者单位: Department of Genetics, Portuguese Oncology Institute, Porto, Portugal [1] Department of Genetics, Portuguese Oncology Institute, Porto, Portugal, Institute of Biomedical [2] Institute of Human Genetics, University Hospital Bonn, Bonn, Germany [3] Department of Radiotherapy, Portuguese Oncology Institute, Porto, Portugal [4] Department of Oncology, Portuguese Oncology Institute, Porto, Portugal [5] Colon Cancer Genetics Group, Institute of Genetics and Molecular Medicine, University of Edinburgh [6] Department of Surgery, S. Jo?o Hospital, Porto, Portugal [7] Department of Gastroenterology, Portuguese Oncology Institute, Porto, Portugal [8] Dept. of Genetic Medicine, Manchester Academic Health Science Centre, Central Manchester Foundation [9] Department of Colorectal Surgery, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina [10] Department of Pathology, Portuguese Oncology Institute, Porto, Portugal [11] Department of Pathology, Portuguese Oncology Institute, Porto, Portugal, Institute of Biomedical [12] Department of Gastroenterology, Centro Hospitalar Tamega e Sousa, Penafiel, Portugal [13]
发布时间 2018-06-23
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Clinical Genetics: An International Journal of Genetics in Medicine

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