Germline MLH1 and MSH2 mutational spectrum including frequent large genomic aberrations in Hungarian hereditary non-polyposis colorectal cancer families: Implications for genetic testing

Lignende værker

• High prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers Syndrome patients
  af: Papp, Janos, et al.
  Udgivet: (2010)
• Detection of hMSH2 and hMLH1 mutations in Chinese hereditary non-polyposis colorectal cancer kindreds
  af: Zhang, Chang-Hua, et al.
  Udgivet: (2008)
• Two novel germline mutations of MLH1 and investigation of their pathobiology in hereditary non-polyposis colorectal cancer families in China
  af: Wang, Chao-Fu, et al.
  Udgivet: (2007)
• Frequent Novel Variations Within MSH2 and MLH1 Genes in a Subset of Iranian Families With Hereditary Non-Polyposis Colorectal Cancer
  af: Shadi Javan, et al.
  Udgivet: (2019-05-01)
• Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutation
  af: Wagner, A, et al.
  Udgivet: (2002)