2008 | MLL rearrangement with t(6;11)(q15;q23) as a sole abnormality in a patient with de novo acute myeloid leukemia: conventional cytogenetics, FISH, and multicolor FISH analyses for detection of rare MLL-related chromosome abnormalities. | CANCER GENETICS AND CYTOGENETICS |
2010 | Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia. | CANCER GENETICS AND CYTOGENETICS |
2017 | Next-generation sequencing of BRCA1/2 in breast cancer patients: potential effects on clinical decision-making using rapid, high-accuracy genetic results
| ANNALS OF SURGICAL TREATMENT AND RESEARCH |
2022 | Next-generation sequencing of molecular tagged circulating cell free DNA of hepatocellular carcinoma | CLINICA CHIMICA ACTA |
2019 | Next-generation sequencing with comprehensive bioinformatics analysis facilitates somatic mosaic APC gene mutation detection in patients with familial adenomatous polyposis
| BMC Medical Genomics |
2015 | NOTCH2 missplicing can occur in relation to apoptosis | BLOOD |
2011 | Osteolytic mandible presenting as an initial manifestation of an adult acute lymphoblastic leukaemia | INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY |
2009 | Oxidative status in iron-deficiency anemia. | JOURNAL OF CLINICAL LABORATORY ANALYSIS |
2008 | Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding analysis. | CANCER GENETICS AND CYTOGENETICS |
2012 | Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect. | CLINICAL GENETICS |
2008 | Preceding orbital granulocytic sarcoma in an adult patient with acute myelogenous leukemia with t(8;21): a case study and review of the literature. | CANCER GENETICS AND CYTOGENETICS |
2010 | Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21). | CANCER GENETICS AND CYTOGENETICS |
2008 | Rare translocations involving chromosome band 8p11 in myeloid neoplasms. | CANCER GENETICS AND CYTOGENETICS |
2022 | Real-world data on prognostic value of measurable residual disease assessment by fragment analysis or next-generation sequencing in multiple myeloma | BRITISH JOURNAL OF HAEMATOLOGY |
2003 | Rifampin 내성 결핵의 진단에서 INNO-LiPA 검사법의 임상적 의미
| TUBERCULOSIS AND RESPIRATORY DISEASES |
2007 | t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma | CANCER GENETICS AND CYTOGENETICS |
2019 | Targeted next generation sequencing can serve as an alternative to conventional tests in myeloid neopla는
| PLOS ONE |
2009 | The clopidogrel resistance can be attenuated with triple antiplatelet therapy in patients undergoing drug-eluting stents implantation | INTERNATIONAL JOURNAL OF CARDIOLOGY |
2009 | Therapy-related acute lymphoblastic leukemia with t(9;22)(q34;q11.2):a case study and review of the literature | CANCER GENETICS AND CYTOGENETICS |
2009 | Therapy-related myelodysplastic syndrome with der(17)t(12;17)(q13;p13) as a new recurrent cytogenetic abnormality after treatment for chronic lymphocytic leukemia | LEUKEMIA RESEARCH |
2009 | Therapy-related myelodysplastic syndrome/acute myeloid leukemia after treatment with temozolomide in a patient with glioblastoma multiforme. | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
2009 | Three-way Philadelphia variant t(9;22;14)(q34;q11.2;p11) in chronic myeloid leukemia. | CANCER GENETICS AND CYTOGENETICS |
2000 | Tissue plasminogen activator and plasminogen activator inhibitor-1 in human choledochal bile
| Yonsei Medical Journal |
2008 | Trisomy 8 in an elderly patient with acute lymphoblastic leukemia as a sole abnormality | CANCER GENETICS AND CYTOGENETICS |
2009 | Two case reports of 1q triplication in myeloproliferative neoplasms. | CANCER GENETICS AND CYTOGENETICS |
2024 | Unraveling trajectories from aplastic anemia to hematologic malignancies: genetic and molecular insights
| FRONTIERS IN ONCOLOGY |
2015 | 천식 치료 중 우연히 발견된 Birt-Hogg-Dube 증후군 1예
| ALLERGY ASTHMA & RESPIRATORY DISEASE |