Loss of Heterozygosity Analysis Using Whole Genome Amplification, Cell Sorting, and Fluorescence-Based PCR

Lignende værker

• Translation of an STR-based biomarker into a clinically compatible SNP-based platform for loss of heterozygosity
  af: Kissel, Heather D., et al.
  Udgivet: (2009)
• Direct Inference of SNP Heterozygosity Rates and Resolution of LOH Detection
  af: Li, Xiaohong, et al.
  Udgivet: (2007)
• Copy number and loss of heterozygosity detected by SNP array of formalin-fixed tissues using whole-genome amplification.
  af: Angela Stokes, et al.
  Udgivet: (2011-01-01)
• Copy Number and Loss of Heterozygosity Detected by SNP Array of Formalin-Fixed Tissues Using Whole-Genome Amplification
  af: Stokes, Angela, et al.
  Udgivet: (2011)
• Clonal Expansion and Loss of Heterozygosity at Chromosomes 9p and 17p in Premalignant Esophageal (Barrett’s) Tissue
  af: Galipeau, Patricia C., et al.
  Udgivet: (1999)