Myungshin Kim
0000-0001-8632-0168
10 papers found
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Clinical Features, Gene Alterations, and Outcomes in Prefibrotic and Overt Primary and Secondary Myelofibrotic Patients
Postoperative Circulating Tumor DNA Can Predict High Risk Patients with Colorectal Cancer Based on Next-Generation Sequencing
Heavy/light chain assay as a biomarker for diagnosis and follow-up of multiple myeloma
Hereditary dehydrated stomatocytosis with splicing site mutation of PIEZO1 mimicking myelodysplastic syndrome diagnosed by targeted next-generation sequencing
Passage-dependent accumulation of somatic mutations in mesenchymal stromal cells during in vitro culture revealed by whole genome sequencing
Practical informativeness of short tandem repeat loci for chimerism analysis in hematopoietic stem cell transplantation
Considerations when using next-generation sequencing for genetic diagnosis of long-QT syndrome in the clinical testing laboratory
Clinical outcomes of venous thromboembolism with dalteparin therapy in multiple myeloma patients
Determination of posaconazole concentration with LC–MS/MS in adult patients with hematologic malignancy
Genetic and epigenetic alterations of bone marrow stromal cells in myelodysplastic syndrome and acute myeloid leukemia patients
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