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Chromosomal Aberrations in Ovarian Carcinoma Cell Line, SNU - S , Using Chromosome Painting

Kang JS, Kim DW, Chun YH, Park SH

  • KMID: 2137119
  • J Korean Cancer Assoc.
  • 2000 Feb;32(1):120-128.
PURPOSE: The characterization of all recognizable chromosomal rearrangements was dis- turbed by technical limitation of conventional cytogenetic methods. Recently, the strong usefullness of generation of chromosome specific painting probes in identification of marker...
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Detection of the Pallister-Killian Syndrome by G-Banding and FISH in Cultured Skin Fibroblasts

Han JY, Kim TG, Shaffer LG, FACMG

  • KMID: 2089519
  • Korean J Clin Pathol.
  • 1998 Jun;18(2):284-287.
Pallister-Killian syndrome is a rare disorder characterized by multiple congenital anomalies, coarse face, profound mental retardation, and epilepsy. Chromosomes of peripheral lymphocytes are usually normal, however, tissue cultures show varying...
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Duplication of intrachromosomal insertion segments 4q32-->q35 confirmed by comparative genomic hybridization and fluorescent in situ hybridization

Kim JW, Park JY, Oh AR, Choi EY, Ryu HM, Kang IS, Koong MK, Park SY

A 35-year-old man with infertility was referred for chromosomal analysis. In routine cytogenetic analysis, the patient was seen to have additional material of unknown origin on the terminal region of...
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Chromosomal Alterations in Gastric Cancer Cell Lines Detected by Comparative Genomic Hybridization

Ha MJ, Park SJ, Kang HW, Kim HJ, Kim HC

  • KMID: 2175217
  • J Korean Cancer Assoc.
  • 1999 Apr;31(2):219-229.
PURPOSE: There are only a few cytogenetic studies in gastric cancer and so far no consistent specific chromosomal abnormalities have been described. In this study, we have used comparative genomic...
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Chromosomal Alterations in Hepatocellular Carcinoma Cell Lines Detected by Comparative Genomic Hybridization

Park SJ, Ha MJ, Kim HC, Kim HJ

  • KMID: 2134351
  • Cancer Res Treat.
  • 2002 Jun;34(3):175-185.
PURPOSE: There have only been a few cytogenetic studies of hepatocellular carcinoma (HCC), and so far, no consistent specific chromosomal abnormalities have been described. Here, we have used comparative genomic...
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