Jaewoo Song

t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma.

A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia.

[Evaluation of the Abbott Cell-Dyn Sapphire hematology analyzer].

Investigation of von Willebrand factor gene mutations in Korean von Willebrand disease patients.

8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with eosinophilia and FGFR1 abnormality.

A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer.

Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding analysis.

Preceding orbital granulocytic sarcoma in an adult patient with acute myelogenous leukemia with t(8;21): a case study and review of the literature.

Complex t(8;19;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia.

Tetrasomy 8 in a patient with acute monoblastic leukemia.

Acute erythroleukemia with der(1;7)(q10;p10) as a sole acquired abnormality after treatment with azathioprine.

Rare translocations involving chromosome band 8p11 in myeloid neoplasms.

[Evaluation of multiplex PCR assay using dual priming oligonucleotide system for detection mutation in the Duchenne muscular dystrophy gene].

Linear relationship between ADAMTS13 activity and platelet dynamics even before severe thrombocytopenia.

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.

Trisomy 8 in an elderly patient with acute lymphoblastic leukemia as a sole abnormality.

Acute promyelocytic leukemia relapsing as secondary acute myelogenous leukemia with translocation t(3;21)(q26;q22) and RUNX1-MDS1-EVI1 fusion transcript.

Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts.

Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer.

Acute promyelocytic leukemia with insertion of PML exon 7a and partial deletion of exon 3 of RARA: a novel variant transcript related to aggressive course and not detected with real-time polymerase chain reaction analysis.

Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21.

Therapy-related myelodysplastic syndrome with der(17)t(12;17)(q13;p13) as a new recurrent cytogenetic abnormality after treatment for chronic lymphocytic leukemia.

JAK2 V617F/C618R mutation in a patient with polycythemia vera: a case study and review of the literature.

Non-age related Y chromosome loss in an elderly patient with acute promyelocytic leukemia.

Detection of a novel CBFB/MYH11 variant fusion transcript (K-type) showing partial insertion of exon 6 of CBFB gene using two commercially available multiplex RT-PCR kits.

A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literature.

BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia.

Concomitant t(3;3)(q21;q26), trisomy 19, and E255V mutation associated with imatinib mesylate resistance in chronic myelogenous leukemia.

der(1)t(1;19)(p13;p13.1) in two elderly patients with myeloid neoplasms: new case reports and review of the literature.

Therapy-related acute lymphoblastic leukemia with t(9;22)(q34;q11.2):a case study and review of the literature.

Three-way Philadelphia variant t(9;22;14)(q34;q11.2;p11) in chronic myeloid leukemia.

Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation.

A novel PHEX mutation in a Korean patient with sporadic hypophosphatemic rickets.

Two case reports of 1q triplication in myeloproliferative neoplasms.

Association between acute promyelocytic leukemia and ring chromosome 6.

Chronic myelomonocytic leukemia with der(9)t(1;9)(q11;q34) as a sole abnormality.

A novel t(1;12)(q21;q24) in a patient with myelodysplastic syndrome.

Detection of FUS-ERG chimeric transcript in two cases of acute myeloid leukemia with t(16;21)(p11.2;q22) with unusual characteristics.

A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family.

CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia.

Therapy-related myelodysplastic syndrome/acute myeloid leukemia after treatment with temozolomide in a patient with glioblastoma multiforme.

Three-way translocation involving MLL, MLLT1, and a novel third partner, NRXN1, in a patient with acute lymphoblastic leukemia and t(2;19;11) (p12;p13.3;q23).

Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia.

Automated detection of malaria-associated pseudoeosinophilia and abnormal WBC scattergram by the Sysmex XE-2100 hematology analyzer: a clinical study with 1,801 patients and real-time quantitative PCR analysis in vivax malaria-endemic area.

Constitutional pericentric inversion 9 in Korean patients with chronic myelogenous leukemia.

Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia.

Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight years.

An SRY-deleted XXY female resulting from a paternally inherited t(Y;22).

Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21).

[Parvovirus B19-induced pure red cell aplasia in a liver transplant recipient].

Diagnosis of non-overt disseminated intravascular coagulation made according to the International Society on Thrombosis and Hemostasis criteria with some modifications.

Elevated levels of activated and inactivated thrombin-activatable fibrinolysis inhibitor in patients with sepsis.

A heparin binding site Arg79Cys missense mutation in the SERPINC1 gene in a Korean patient with hereditary antithrombin deficiency.

Acute promyelocytic leukemia with trisomy 8 and del(9)(q22) after treatment of cervical cancer with concurrent chemoradiotherapy: a case report.

Delta neutrophil index: a promising diagnostic and prognostic marker for sepsis.

CD5-negative blastoid variant mantle cell lymphoma with complex CCND1/IGH and MYC aberrations.

A Gly1609Arg missense mutation in the vWF gene in a Korean patient with von Willebrand disease type 2A.

Fibrinogen residue γAla341 is necessary for calcium binding and 'A-a' interactions.

Comparison study of the rates of manual peripheral blood smear review from 3 automated hematology analyzers, Unicel DxH 800, ADVIA 2120i, and XE 2100, using international consensus group guidelines.

An engineered fibrinogen variant AαQ328,366P does not polymerise normally, but retains the ability to form α cross-links.

Immature platelet fraction in diabetes mellitus and metabolic syndrome.

Comparison of prothrombin time derived from CoaguChek XS and laboratory test according to fibrinogen level.

The instability of commercial control materials in quality control of mean corpuscular volume.

Analytical and clinical performance of a new point of care LABGEOIB D-dimer test for diagnosis of venous thromboembolism.

Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure.

Capillary-scale direct measurement of hemoglobin concentration of erythrocytes using photothermal angular light scattering.

Quantitative Influence of ABO Blood Groups on Factor VIII and Its Ratio to von Willebrand Factor, Novel Observations from an ARIC Study of 11,673 Subjects.

Clinical Utility of Bone Marrow Study in Gaucher Disease: A Case Report of Gaucher Disease Type 3 With Intractable Myoclonic Seizures.

Automated CH50 liposome-based immunoassay: consideration in dilution and validation of reference interval.

Magnetic bead-based nucleic acid purification kit: Clinical application and performance evaluation in stool specimens.

Association of Single Nucleotide Polymorphisms in the ST3GAL4 Gene with VWF Antigen and Factor VIII Activity.