Dept. of Laboratory Medicine

Issue DateTitleYonsei Author(s)
2011A heparin binding site Arg79Cys missense mutation in the SERPINC1 gene in a Korean patient with hereditary antithrombin deficiency., et al
2014A Korean Patient with Lattice Corneal Dystrophy Type IV with Leu527Arg Mutation in the TGFBI Gene, et al
2016A multicenter phase II study of sorafenib in combination with erlotinib in patients with advanced non-small cell lung cancer (KCSG-0806), et al
2009A new automated multiple allergen simultaneous test-chemiluminescent assay (MAST-CLA) using an AP720S analyzer, et al
2015A new HLA-B*15 allele, HLA-B*15:263, identified in a Korean individual, et al
2002A new integron carrying VIM-2 metallo-β-lactamase gene cassette in a Serratia marcescens isolate., et al
2008A novel bla(CTX-M-14) gene-harboring complex class 1 integron with an In4-like backbone structure from a clinical isolate of Escherichia coli, et al
2006A novel ceftazidime-hydrolysing extended-spectrum β-lactamase, CTX-M-54, with a single amino acid substitution at position 167 in the omega loop, et al
2008A novel de novo mutation in the serine-threonine kinase STK11 gene in a Korean patient with Peutz-Jeghers syndrome, et al
2013A novel F11 mutation in a Korean pediatric patient with recurrent epistaxis, et al
2006A novel fibrinogen variant (fibrinogen Seoul II; AαGln328Pro) characterized by impaired fibrin α-chain cross-linking, et al
2011A novel frameshift mutation at codon 66 (HBB:c.del201A) in the β-globin gene leads to beta-thalassemia, et al
2009A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family, et al
2011A novel insertion sequence, ISAba10, inserted into ISAba1 adjacent to the bla(OXA-23) gene and disrupting the outer membrane protein gene carO in Acinetobacter baumannii, et al
2008A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer., et al
2002A novel missense mutation (I344K) in the SPG4 gene in a Korean family with autosomal-dominant hereditary spastic paraplegia, et al
2012A novel multiplex real-time PCR assay for the concurrent detection of hepatitis A, B and C viruses in patients with acute hepatitis, et al
2011A novel mutation in the MECP2 gene in a Korean patient with Rett syndrome, et al
2009A novel PHEX mutation in a Korean patient with sporadic hypophosphatemic rickets., et al
2011A novel PTEN mutation in a Korean patient with Cowden syndrome and vascular anomalies, et al

Browse