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Ethnic differences in gastric cancer genetic susceptibility: allele flips of interleukin geneAutomated 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.A novel association between relaxin receptor polymorphism and hematopoietic stem cell yield after mobilization.Three cases of manifesting female carriers in patients with Duchenne muscular dystrophyNon-syndromic hearing loss caused by the dominant cis mutation R75Q with the recessive mutation V37I of the GJB2 (Connexin 26) gene.Routine chromosomal microarray analysis is necessary in Korean patients with unexplained developmental delay/mental retardation/autism spectrum disorder.Identification of cell morphology parameters from automatic hematology analyzers to predict the peripheral blood CD34-positive cell count after mobilization.A case of late-onset Li-Fraumeni-like syndrome with unilateral breast cancerDistinct linkage disequilibrium (LD) runs of single nucleotide polymorphisms and microsatellite markers; implications for use of mixed marker haplotypes in LD-based mapping.PRSS1, SPINK1, CFTR, and CTRC Pathogenic Variants in Korean Patients With Idiopathic PancreatitisJAK2 V617F/C618R mutation in a patient with polycythemia vera: a case study and review of the literature.Multiplex Ligation-Dependent Probe Amplification in X-linked Recessive Muscular Dystrophy in Korean Subjects.Analytical Performance of Multiplex Real-Time PCR for Six Sexually Transmitted Pathogens.Prevalence of sexually transmitted infections among healthy Korean women: implications of multiplex PCR pathogen detection on antibiotic therapy.Cerebellar vermis hypoplasia in CHARGE syndrome: clinical and molecular characterization of 18 unrelated Korean patients.Validation and optimization of the Ion Torrent S5 XL sequencer and Oncomine workflow for BRCA1 and BRCA2 genetic testing.Assessment of real-time PCR method for detection of EGFR mutation using both supernatant and cell pellet of malignant pleural effusion samples from non-small-cell lung cancer patients.Novel and Recurrent ACADS Mutations and Clinical Manifestations Observed in Korean Patients with Short-chain Acyl-coenzyme a Dehydrogenase Deficiency.Evaluation of three automated nucleic acid extraction systems for identification of respiratory viruses in clinical specimens by multiplex real-time PCR.Rare Korean Cases of Very-long-chain Acyl-CoA Dehydrogenase Deficiency with a Novel Recurrent Mutation.CD5-negative blastoid variant mantle cell lymphoma with complex CCND1/IGH and MYC aberrations.Partial Gene Deletions of PMP22 Causing Hereditary Neuropathy with Liability to Pressure Palsies.Breakpoint mapping by whole genome sequencing identifies PTH2R gene disruption in a patient with midline craniosynostosis and a de novo balanced chromosomal rearrangement.Bone marrow hypoplasia, isochromosome 8q and deletion of chromosome 6q preceding B-cell lymphoma.Concomitant AID Expression and BCL7A Loss Associates With Accelerated Phase Progression and Imatinib Resistance in Chronic Myeloid Leukemia.Profiling cancer-associated genetic alterations and molecular classification of cancer in Korean gastric cancer patients.Cys482Trp missense mutation in the coagulation factor XI gene (F11) in a Korean patient with factor XI deficiency.First Korean case of SATB2-associated 2q32-q33 microdeletion syndrome.Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations.Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect.Becker muscular dystrophy with r(X) carrying an out-of-frame DMD deletion.Effectiveness of in silico tagSNP selection methods: virtual analysis of the genotypes of pharmacogenetic genes.Differential association of RANTES-403 and IL-1B-1464 polymorphisms on histological subtypes in male Korean patients with gastric cancer.Interleukin 10 polymorphisms differentially influence the risk of gastric cancer in East Asians and Caucasians.Three-way Philadelphia variant t(9;22;14)(q34;q11.2;p11) in chronic myeloid leukemia.A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer.Interaction of polymorphisms in the interleukin 1B-31 and general transcription factor 2A1 genes on the susceptibility to gastric cancer.[Evaluation of multiplex PCR assay using dual priming oligonucleotide system for detection mutation in the Duchenne muscular dystrophy gene].ALK-positive anaplastic large cell lymphoma with TPM3-ALK translocation.A Comparative Study for Detection of EGFR Mutations in Plasma Cell-Free DNA in Korean Clinical Diagnostic Laboratories.
P50
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P50
description
researcher ORCID ID = 0000-0001-5320-6705
@en
name
Kyung-A Lee
@ast
Kyung-A Lee
@en
Kyung-A Lee
@es
Kyung-A Lee
@nl
type
label
Kyung-A Lee
@ast
Kyung-A Lee
@en
Kyung-A Lee
@es
Kyung-A Lee
@nl
prefLabel
Kyung-A Lee
@ast
Kyung-A Lee
@en
Kyung-A Lee
@es
Kyung-A Lee
@nl
P31
P496
0000-0001-5320-6705