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机译:体质性 CHEK2 基因突变携带者发生原发性血小板增多症的风险
Department of Clinical Genetics, Collegium Medicum, Nicolaus Copernicus University, M. Sklodowska;
Department of Hematology, Oncology and Bone Marrow Transplantation, Medical University, Wroclaw;
Department of Hematology, Municipal Hospital, Toruń, Poland;
Congenital CHEK2 mutations; Essential thrombocythemia;
机译:Non-driver gene mutation analysis in a large cohort of polycythemia vera and essential thrombocythemia
机译:Thrombophilic Risk of Factor V Leiden, Prothrombin G20210A, MTHFR, and Calreticulin Mutations in Essential Thrombocythemia Egyptian Patients
机译:Missense mutations (p.H371Y, p.D438Y) in gene CHEK2 are associated with breast cancer risk in women of Balochistan origin
机译:BRCA1 / 2突变携带者的诊断性放射线暴露和乳腺癌风险:回顾性队列研究(GENE-RAD-RISK)
机译:The methylenetetrahydrofolate reductase C677T mutation induces cell-specific changes in genomic DNa methylation and uracil misincorporation: a possible molecular basis for the site-specific cancer risk modification