Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability

Những quyển sách tương tự

• Compound heterozygosity for two MSH2 mutations suggests mild consequences of the initiation codon variant c.1A>G of MSH2
  Bằng: Kets, Carolien M, et al.
  Được phát hành: (2009)
• Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutation
  Bằng: Wagner, A, et al.
  Được phát hành: (2002)
• Genomic rearrangements of hMSH6 contribute to the genetic predisposition in suspected hereditary non-polyposis colorectal cancer syndrome
  Bằng: Plaschke, J, et al.
  Được phát hành: (2003)
• Association of Hereditary Nonpolyposis Colorectal Cancer–Related Tumors Displaying Low Microsatellite Instability with MSH6 Germline Mutations
  Bằng: Wu, Ying, et al.
  Được phát hành: (1999)
• Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer
  Bằng: Verma, L., et al.
  Được phát hành: (1999)