MSH2 genomic deletions are a frequent cause of HNPCC (Q62977773)

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7 December 2019

title

MSH2 genomic deletions are a frequent cause of HNPCC (English)

1 reference

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7 December 2019

1 reference

1

1 reference

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7 December 2019

Hans Vasen

3

1 reference

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7 December 2019

Dick Lindhout

8

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7 December 2019

Riccardo Fodde

10

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7 December 2019

Marjolein van der Klift

2

object named as

van der Klift H

1 reference

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7 December 2019

author name string

Khan PM

4

1 reference

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7 December 2019

Menko F

5

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7 December 2019

Tops C

6

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7 December 2019

Meijers Heijboer H

7

1 reference

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7 December 2019

Møller P

9

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7 December 2019

language of work or name

English

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publication date

1 December 1998

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7 December 2019

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7 December 2019

volume

20

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7 December 2019

issue

4

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7 December 2019

page(s)

326-328

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Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review

7 December 2019

cites work

1 reference

7 January 2021

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

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7 January 2021

Mutation of a mutL homolog in hereditary colon cancer

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7 January 2021

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer

1 reference

7 January 2021

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

1 reference

7 January 2021

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

1 reference

7 January 2021

Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer

1 reference

7 January 2021

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations

1 reference

7 January 2021

Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

1 reference

7 January 2021

Founding mutations and Alu-mediated recombination in hereditary colon cancer

1 reference

7 January 2021

Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability

1 reference

7 January 2021

Monoallelic mutation analysis (MAMA) for identifying germline mutations

1 reference

7 January 2021

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

1 reference

7 January 2021