机译:急性白血病窝藏kmt2a / mllt10 kmt2a / mllt10融合:单个基因组学实验室的10年体验
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
Center for Individualized Medicine‐Biomarker DiscoveryMayo ClinicRochester Minnesota;
Center for Individualized Medicine‐Biomarker DiscoveryMayo ClinicRochester Minnesota;
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
Division of Laboratory Genetics and Genomics Department of Laboratory Medicine and PathologyMayo;
acute myeloid leukemia; acute lymphoblastic leukemia; KMT2A rearrangements; KMT2A/MLLT10 fusion; fluorescence in situ hybridization; mate‐pair sequencing;
机译:急性白血病窝藏kmt2a / mllt10 kmt2a / mllt10融合:单个基因组学实验室的10年体验
机译:隐秘复发acin1 acin1 - Numm1 Nutm1 Numm1融合在非-mt2a kmt2a -rearranged婴儿急性淋巴细胞白血病
机译:一种新型KMT2A-ACTN2 KMT2A-ACTN2婴儿B细胞急性淋巴细胞白血病融合
机译:砷救生优于化疗和骨髓移植复发急性突出细胞细胞白血病:来自香港的十年经验
机译:11Q23中的治疗诱导缺失导致KMT2a与Arhgef12融合并在治疗的儿童中发育B族急性淋巴相血肿由T(9; 11)(p21; Q23)/ kmt2a-mllt3引起的急性髓性白血病进行治疗
机译:MLT10和IL3在具有早期T细胞前体急性淋巴细胞白血病的患者中与复杂的四路易位和三术4一起重新排列:案例报告