Literature DB >> 8695231

MSH2 sequence variations and inherited colorectal cancer susceptibility.

N J Froggatt, J A Joyce, D G Evans, P W Lunt, D J Koch, B J Ponder, E R Maher.   

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Year:  1996        PMID： 8695231     DOI： 10.1016/0959-8049(95)00464-5

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN： 0959-8049            Impact factor:   9.162


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  3 in total

1.  Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer.

Authors:  I P Tomlinson; N E Beck; T Homfray; C J Harocopos; W F Bodmer
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

Review 2.  A mobile threat to genome stability: The impact of non-LTR retrotransposons upon the human genome.

Authors:  Miriam K Konkel; Mark A Batzer
Journal:  Semin Cancer Biol       Date:  2010-03-20       Impact factor: 15.707

3.  Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing.

Authors:  M Cravo; A J Afonso; P Lage; C Albuquerque; L Maia; C Lacerda; P Fidalgo; P Chaves; C Cruz; C Nobre-Leitão
Journal:  Gut       Date:  2002-03       Impact factor: 23.059
  3 in total

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