Browsing by Keyword : In Situ Hybridization, Fluorescence

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Showing results 1 to 12 of 12

Pub YearTitleAuthor(s)
2011Acquisition of a BCR-ABL1 transcript in a patient with disease progression from MDS with fibrosis to AML with myelodysplasia-related changes.김현주, 김효철, 박준성, 이현우, 정성현, 조성란
2010Acute myeloid leukemia with t(16;21)(q24;q22) and eosinophilia: case report and review of the literature.김현주, 박일중, 박준은, 이위교, 조성란
2011Acute promyelocytic leukemia with complex translocation t(5;17;15)(q35;q21;q22): case report and review of the literature.김현주, 박일중, 박준은, 정현주, 조성란
2000Assignment of the kinesin family member 4 genes (KIF4A and KIF4B) to human chromosome bands Xq13.1 and 5q33.1 by in situ hybridization.김완기, 김현주, 이영미, 하만준
2013Clinical and genetic spectrum of 18 unrelated Korean patients with Sotos syndrome: frequent 5q35 microdeletion and identification of four novel NSD1 mutations.손영배, 정선용, 진현석
1998Extensive analysis of duplicated-inverted hepatitis B virus integrations in human hepatocellular carcinoma.윤정구
2015Faggot-like cells observed in acute myeloid leukemia with myelodysplasia-related changes mimicking acute promyelocytic leukemia.박준성, 조성란, 최용원
2016Minor BCR-ABL1-Positive Acute Myeloid Leukemia Associated With the NPM1 Mutation and FLT3 Internal Tandem Duplication정성현, 조성란, 한재호
2010Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia.조성란
2005Myxoid clear cell sarcoma.김유찬
2010Partial tetrasomy of chromosome 22q11.1 resulting from a supernumerary isodicentric marker chromosome in a boy with cat-eye syndrome.고정민, 배기수
2016Skin Barrier Function Is Not Impaired and Kallikrein 7 Gene Polymorphism Is Frequently Observed in Korean X-linked Ichthyosis Patients Diagnosed by Fluorescence in Situ Hybridization and Array Comparative Genomic Hybridization손영배
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