(Q54703592)

3 June 2018

title

A large MSH2 Alu insertion mutation causes HNPCC in a German kindred. (English)

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3 June 2018

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3

Nicolas Wentzensen

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Magnus von Knebel Doeberitz

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7

object named as

Magnus von Knebel Doeberitz

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3 June 2018

author name string

Matthias Kloor

1

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3 June 2018

Christian Sutter

2

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Friedrich W Cremer

4

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Annick Buckowitz

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Monika Keller

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Johannes Gebert

8

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3 June 2018

publication date

31 August 2004

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3 June 2018

published in

Human Genetics

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3 June 2018

volume

115

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3 June 2018

issue

5

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page(s)

432-438

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3 June 2018

https://scigraph.springernature.com/pub.10.1007/s00439-004-1176-9

exact match

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Mismatch repair and the hereditary non-polyposis colorectal cancer syndrome (HNPCC)

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12 December 2020

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A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots

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12 December 2020

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12 December 2020

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

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12 December 2020

Mismatch repair genes hMLH1 and hMSH2 and colorectal cancer: a HuGE review

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12 December 2020

Insertion of a short Alu sequence into the hMSH2 gene following a double cross over next to sequences with chi homology

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Mutational inactivation of the proapoptotic gene BAX confers selective advantage during tumor clonal evolution

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The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors

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Molecular screening of potential HNPCC patients using a multiplex microsatellite PCR system

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Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.

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Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

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Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

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Alu repeats and human genomic diversity

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De novo insertion of an Alu sequence in the coding region of the CLCN5 gene results in Dent's disease

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12 December 2020

10.1007/S00439-004-1176-9

Identifiers

DOI

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3 June 2018

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3 June 2018