Browsing by Yonsei Author : Lee, Kyung A

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Name:
Lee, Kyung A [이경아]
orcid http://orcid.org/0000-0001-5320-6705
Department :
College of Medicine (의과대학) - Dept. of Laboratory Medicine (진단검사의학교실)
Scopus ID :
Scopus (56275385700)

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Showing results 101 to 150 of 201

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Issue DateTitleJournal Title
2012A novel three-way variant t(4;17;5)(p16;q23;q31) in a case of secondary plasma cell leukemia.LEUKEMIA RESEARCH
2012Refractory anemia with ring sideroblasts associated with marked thrombocytosis harboring cytogenetic abnormality dup(2)(p15p22) treated with decitabine.LEUKEMIA & LYMPHOMA
2012Novel in-frame deletion mutation in FLCN gene in a Korean family with recurrent primary spontaneous pneumothorax.GENE
2012Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect.CLINICAL GENETICS
2012CD5-negative blastoid variant mantle cell lymphoma with complex CCND1/IGH and MYC aberrations ANNALS OF LABORATORY MEDICINE
2012A Gly1609Arg missense mutation in the vWF gene in a Korean patient with von Willebrand disease type 2AANNALS OF CLINICAL AND LABORATORY SCIENCE
2011PARD Syndrome with PTPN11 Gene Mutation Showing Six Cardinal Symptoms of LEOPARD ANNALS OF DERMATOLOGY
2011Acute promyelocytic leukemia with trisomy 8 and del(9)(q22) after treatment of cervical cancer with concurrent chemoradiotherapy: a case report.ONKOLOGIE
2011Rapid identification of thrombocytopenia-associated multiple organ failure using red blood cell parameters and a volume/hemoglobin concentration cytogram YONSEI MEDICAL JOURNAL
2011A heparin binding site Arg79Cys missense mutation in the SERPINC1 gene in a Korean patient with hereditary antithrombin deficiency.ANNALS OF CLINICAL AND LABORATORY SCIENCE
2011Cytochrome P450 2C19 polymorphism is associated with reduced clopidogrel response in cerebrovascular disease. YONSEI MEDICAL JOURNAL
2011Three cases of manifesting female carriers in patients with Duchenne muscular dystrophy. YONSEI MEDICAL JOURNAL
2011A novel PTEN mutation in a Korean patient with Cowden syndrome and vascular anomalies ACTA DERMATO-VENEREOLOGICA
2010Cytogenetic features of 5q deletion and 5q- syndrome in myelodysplastic syndrome in Korea; marker chromosomes proved to be chromosome 5 with interstitial deletion by fluorescence in situ hybridizationCANCER GENETICS AND CYTOGENETICS
2010Association between survivor motor neuron 2 (SMN2) gene homozygous deletion and sporadic lower motor neuron disease in a Korean population.ANNALS OF CLINICAL AND LABORATORY SCIENCE
2010A case of pseudoisodicentric chromosome 18q detected at prenatal diagnosis KOREAN JOURNAL OF LABORATORY MEDICINE
2010Ambras syndrome in a Korean patient with balanced pericentric inversion (8)(p11.2q24.2).JOURNAL OF DERMATOLOGICAL SCIENCE
2010Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight yearsANNALS OF CLINICAL AND LABORATORY SCIENCE
2010Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia.CANCER GENETICS AND CYTOGENETICS
2010An SRY-deleted XXY female resulting from a paternally inherited t(Y;22)ANNALS OF CLINICAL AND LABORATORY SCIENCE
2010Down-Turner syndrome (45,X/47,XY,+21): case report and review KOREAN JOURNAL OF LABORATORY MEDICINE
2010Determination of SMN1 and SMN2 copy numbers in a Korean population using multiplex ligation-dependent probe amplification KOREAN JOURNAL OF LABORATORY MEDICINE
2010Interleukin 10 polymorphisms differentially influence the risk of gastric cancer in East Asians and CaucasiansCYTOKINE
2010Automated 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 AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE
2010Three-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).CANCER GENETICS AND CYTOGENETICS
2010Multiplex Ligation-dependent Probe Amplification (MLPA) 방법에 의한 디스트로핀 유전자 돌연변이 분자학적 진단의 유용성 Journal of the Korean Neurological Association
2009Three-way Philadelphia variant t(9;22;14)(q34;q11.2;p11) in chronic myeloid leukemia.CANCER GENETICS AND CYTOGENETICS
2009CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemiaCANCER GENETICS AND CYTOGENETICS
2009De novo interstitial direct duplication 8 (p21.3p23.1) with Pierre Robin sequence Korean Journal of Pediatrics
2009Detection of FUS-ERG chimeric transcript in two cases of acute myeloid leukemia with t(16;21)(p11.2;q22) with unusual characteristics.CANCER GENETICS AND CYTOGENETICS
2009The First Korean Case of Camurati-Engelmann Disease (Progressive Diaphyseal Dysplasia) Confirmed by TGFB1 Gene Mutation Analysis JOURNAL OF KOREAN MEDICAL SCIENCE
2009Clinical Significance of von Willebrand Factor-Cleaving Protease (ADAMTS13) Deficiency in Patients with Sepsis-Induced Disseminated Intravascular Coagulation INFECTION AND CHEMOTHERAPY (감염과 화학요법)
2009BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia.CANCER GENETICS AND CYTOGENETICS
2009A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literatureCANCER GENETICS AND CYTOGENETICS
2009Detection 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 kitsCANCER GENETICS AND CYTOGENETICS
2009Concomitant t(3;3)(q21;q26), trisomy 19, and E255V mutation associated with imatinib mesylate resistance in chronic myelogenous leukemiaCANCER GENETICS AND CYTOGENETICS
2009Two case reports of 1q triplication in myeloproliferative neoplasms.CANCER GENETICS AND CYTOGENETICS
2009A novel PHEX mutation in a Korean patient with sporadic hypophosphatemic rickets.ANNALS OF CLINICAL AND LABORATORY SCIENCE
2009Therapy-related acute lymphoblastic leukemia with t(9;22)(q34;q11.2):a case study and review of the literatureCANCER GENETICS AND CYTOGENETICS
2009Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA).THROMBOSIS RESEARCH
2009JAK2 V617F/C618R mutation in a patient with polycythemia vera: a case study and review of the literatureCANCER GENETICS AND CYTOGENETICS
2009Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcriptsCANCER GENETICS AND CYTOGENETICS
2009Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21CANCER GENETICS AND CYTOGENETICS
2009Acute 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 analysisCANCER GENETICS AND CYTOGENETICS
2009Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancerCANCER GENETICS AND CYTOGENETICS
2008MLL 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
2008Paracentric 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
20088번 염색체 사체성을 보인 급성단구성백혈병 1예 KOREAN JOURNAL OF LABORATORY MEDICINE
2008Becker muscular dystrophy with r(X) carrying an out-of-frame DMD deletionPEDIATRIC NEUROLOGY
2008A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer.CANCER GENETICS AND CYTOGENETICS

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