| 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 | A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family | BLOOD COAGULATION & FIBRINOLYSIS |
| 2009 | Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA). | THROMBOSIS RESEARCH |
| 2009 | JAK2 V617F/C618R mutation in a patient with polycythemia vera: a case study and review of the literature | CANCER GENETICS AND CYTOGENETICS |
| 2009 | The relationship between COL3A1 exon 31 polymorphism and pelvic organ prolapse. | JOURNAL OF UROLOGY |
| 2009 | Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts | CANCER GENETICS AND CYTOGENETICS |
| 2009 | Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21 | CANCER GENETICS AND CYTOGENETICS |
| 2009 | 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 | CANCER GENETICS AND CYTOGENETICS |
| 2009 | Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer | CANCER GENETICS AND CYTOGENETICS |
| 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 |
| 2008 | 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. | CANCER GENETICS AND CYTOGENETICS |
| 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 |
| 2008 | 8번 염색체 사체성을 보인 급성단구성백혈병 1예
| KOREAN JOURNAL OF LABORATORY MEDICINE |
| 2008 | Becker muscular dystrophy with r(X) carrying an out-of-frame DMD deletion | PEDIATRIC NEUROLOGY |
| 2008 | A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer. | CANCER GENETICS AND CYTOGENETICS |
| 2008 | Acute promyelocytic leukemia relapsing as secondary acute myelogenous leukemia with translocation t(3;21)(q26;q22) and RUNX1-MDS1-EVI1 fusion transcript | CANCER GENETICS AND CYTOGENETICS |
| 2008 | 듀센형근이영양증 유전자의 결실 돌연변이 검출을 위한 Dual Priming Oligonucleotide 다중 PCR법의 평가
| KOREAN JOURNAL OF LABORATORY MEDICINE |
| 2008 | Trisomy 8 in an elderly patient with acute lymphoblastic leukemia as a sole abnormality | CANCER GENETICS AND CYTOGENETICS |
| 2008 | Rare translocations involving chromosome band 8p11 in myeloid neoplasms. | CANCER GENETICS AND CYTOGENETICS |
| 2008 | Linear relationship between ADAMTS13 activity and platelet dynamics even before severe thrombocytopenia | ANNALS OF CLINICAL AND LABORATORY SCIENCE |
| 2008 | Acute erythroleukemia with der(1;7)(q10;p10) as a sole acquired abnormality after treatment with azathioprine. | CANCER GENETICS AND CYTOGENETICS |
| 2008 | Complex t(8;19;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia | CANCER GENETICS AND CYTOGENETICS |
| 2008 | A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome
| BMC MEDICAL 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 |
| 2007 | Investigation of von Willebrand factor gene mutations in Korean von Willebrand disease patients
| KOREAN JOURNAL OF LABORATORY MEDICINE |
| 2007 | 자동혈구분석기 Cell-Dyn Sapphire의 평가
| KOREAN JOURNAL OF LABORATORY MEDICINE |
| 2007 | A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia | CANCER GENETICS AND CYTOGENETICS |
| 2007 | t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma | CANCER GENETICS AND CYTOGENETICS |
| 2006 | Fibrinogen Seoul (FGG Ala341Asp): A novel mutation associated with hypodysfibrinogenemia | CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS |
| 2006 | Clinical evaluation of micro-scale chip-based PCR system for rapid detection of hepatitis B virus | BIOSENSORS & BIOELECTRONICS |
| 2006 | Plasma level of IL-6 and its relationship to procoagulant and fibrinolytic markers in acute ischemic stroke
| YONSEI MEDICAL JOURNAL |
| 2006 | GnRH (Gonadotropin-Releasing Hormone)에 의한 자궁내막암 유래 세포주의 세포 증식 억제 기전에 있어서 Integrin, FAK (FocalAdhesion Kinase) 및 ERK (Extracellular Signal Regulated Kinase)의 역할
| Korean Journal of the Fertility and Sterility |
| 2006 | Plasma factor XIII activity in patients with disseminated intravascular coagulation
| YONSEI MEDICAL JOURNAL |
| 2006 | A novel fibrinogen variant (fibrinogen Seoul II; AαGln328Pro) characterized by impaired fibrin α-chain cross-linking
| BLOOD |
| 2005 | Homozygous type I Protein C deficiency in neonatal purpura fulminans with a novel frame-shift deletion of 10 base pairs in exon 8 of PROC gene | JOURNAL OF THROMBOSIS AND HAEMOSTASIS |
| 2005 | Effectiveness of Real-Time Quantitative PCR Compare to Repeat PCR for the Diagnosis of Charcot-Marie-Tooth Type 1A and Hereditary Neuropathy with Liability to Pressure Palsies
| YONSEI MEDICAL JOURNAL |
| 2004 | CMV 질환의 면역치료법 개발에 대한 최신지견 | Konkuk Journal of Medical Sciences (건국의과학학술지) |
| 2004 | Epidemiological characteristics and molecular basis of fluoroquinolone-resistant Neisseria gonorrhoeae strains isolated in Korea and nearby countries
| JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY |
| 2004 | Adoptive Immunotherapy for Cytomegalovirus (CMV) Disease in Immunocompromised Patients
| YONSEI MEDICAL JOURNAL |
| 2003 | Detection of an Ala601Thr Mutation of Plasminogen Gene in 3 out of 36 Korean Patients with Deep Vein Thrombosis
| JOURNAL OF KOREAN MEDICAL SCIENCE |
| 2003 | Rifampin 내성 결핵의 진단에서 INNO-LiPA 검사법의 임상적 의미
| TUBERCULOSIS AND RESPIRATORY DISEASES |
| 2002 | Evaluation of HER2/neu Status by Real-Time Quantitative PCR in Breast Cancer
| YONSEI MEDICAL JOURNAL |
| 2001 | A Novel Silent Substitution (C8516T) in Exon 9 of the Human PROC Gene
| YONSEI MEDICAL JOURNAL |
| 2001 | Homozygous V/V (677C to T) and D/D (2756G to A) variants in the methylenetetrahydrofolate and methionine synthase genes in a case of hyperhomocysteinemia with stroke at young age
| EXPERIMENTAL AND MOLECULAR MEDICINE |
| 2001 | Presence of 844ins68 in the cystathionine beta-synthase gene in Asians (Koreans) | THROMBOSIS AND HAEMOSTASIS |
| 2001 | A Case of del(13)(q22) with Multiple Major Congenital Anomalies, Imperforate Anus and Penoscrotal Transposition
| YONSEI MEDICAL JOURNAL |
| 2000 | Tissue plasminogen activator and plasminogen activator inhibitor-1 in human choledochal bile
| Yonsei Medical Journal |
| 2000 | A case of Klinefelter syndrome with retroperitoneal teratoma
| Yonsei Medical Journal |
| 1999 | von Willebrand disease with G4022A mutation (vWd Sungnam): a case report
| Journal of Korean Medical Science |
| 1999 | Absence of the prothrombin gene variant in Koreans | Thrombosis and Haemostasis |
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