Literature DB >> 3940919

Frequency of hereditary nonpolyposis colorectal carcinoma (Lynch syndromes I and II).

H T Lynch.   

Abstract

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Year:  1986        PMID： 3940919     DOI： 10.1016/0016-5085(86)90952-2

Source DB:  PubMed          Journal:  Gastroenterology        ISSN： 0016-5085            Impact factor:   22.682


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  6 in total

1.  An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation.

Authors:  Angela Arnold; Stewart Payne; Samantha Fisher; Diane Fricker; Judith Soloway; Susan M White; Marco Novelli; Kylie MacDonald; James Mackay; Richard Groves; Natalie Canham
Journal:  Fam Cancer       Date:  2007-02-24       Impact factor: 2.375

2.  Frequency of hereditary nonpolyposis colorectal cancer in southern Alberta.

Authors:  P J Westlake; H E Bryant; S A Huchcroft; L R Sutherland
Journal:  Dig Dis Sci       Date:  1991-10       Impact factor: 3.199

3.  How prevalent is cancer family syndrome?

Authors:  F Kee; B J Collins
Journal:  Gut       Date:  1991-05       Impact factor: 23.059

Review 4.  Hereditary nonpolyposis colorectal cancer (Lynch syndrome): criteria for identification and management.

Authors:  Gregory Kouraklis; Evangelos P Misiakos
Journal:  Dig Dis Sci       Date:  2005-02       Impact factor: 3.199

5.  Colorectal cancer in patients with family history.

Authors:  M Conio; L Bonelli; H Martines; F Petrogalli; H Aste; L Santi
Journal:  Int J Colorectal Dis       Date:  1987-11       Impact factor: 2.571

Review 6.  Multiple genetic alterations in human carcinogenesis.

Authors:  T Sugimura; M Terada; J Yokota; S Hirohashi; K Wakabayashi
Journal:  Environ Health Perspect       Date:  1992-11       Impact factor: 9.031
  6 in total

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