(Q44837117)

6 December 2017

Deciphering the colon cancer genes--report of the InSiGHT-Human Variome Project Workshop, UNESCO, Paris 2010. (English)

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6 December 2017

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6 December 2017

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20

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6 December 2017

Maurizio Genuardi

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Amanda Spurdle

object named as

Amanda B Spurdle

21

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Annika Lindblom

15

object named as

Annika Lindblom

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6 December 2017

16

Donna Maglott

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6 December 2017

13

Elke Holinski-Feder

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6 December 2017

17

Pål Møller

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6 December 2017

2

Finlay Macrae

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6 December 2017

Maija R J Kohonen-Corish

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6 December 2017

Stefan Aretz

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6 December 2017

Bharati Bapat

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6 December 2017

Inge T Bernstein

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6 December 2017

Richard G H Cotton

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6 December 2017

Johan T den Dunnen

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6 December 2017

Thierry Frebourg

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6 December 2017

Marc S Greenblatt

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6 December 2017

Hans Morreau

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6 December 2017

Gabriela Möslein

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6 December 2017

Sean Tavtigian

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6 December 2017

Carli M J Tops

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6 December 2017

Thomas K Weber

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6 December 2017

Niels de Wind

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6 December 2017

Michael O Woods

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6 December 2017

Contributors to the InSiGHT-HVP Workshop

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6 December 2017

8 March 2011

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6 December 2017

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6 December 2017

32

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6 December 2017

4

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6 December 2017

491-494

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Classifying MLH1 and MSH2 variants using bioinformatic prediction, splicing assays, segregation, and tumor characteristics

6 December 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR).

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

Report of the combined meeting of the International Society for Gastrointestinal Hereditary Tumours, the Human Variome Project and the National Cancer Institute Colon Cancer Family Registry, Duesseldorf, Germany, 24 June 2009.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

Clinical relevance of rare germline sequence variants in cancer genes: evolution and application of classification models

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

A database to support the interpretation of human mismatch repair gene variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

A new variant database for mismatch repair genes associated with Lynch syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21450

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/HUMU.21450

1 reference

6 December 2017

1 reference