(Q48276381)

10 February 2018

title

Different molecular mechanisms underlie genomic deletions in the MLH1 Gene (English)

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10 February 2018

author

Maurizio Ponz de Leon

9

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10 February 2018

Valentina Rovella

Valentina Rovella

7

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Emanuela Lucci Cordisco

Emanuela Lucci-Cordisco

4

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Salvatore Pucciarelli

Salvatore Pucciarelli

6

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Alessandra Viel

Alessandra Viel

1

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Maurizio Genuardi

Maurizio Genuardi

11

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author name string

Fiorella Petronzelli

2

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10 February 2018

Lara Della Puppa

3

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10 February 2018

Mara Fornasarig

5

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10 February 2018

Michele Quaia

8

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10 February 2018

Mauro Boiocchi

10

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10 February 2018

publication date

1 November 2002

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10 February 2018

published in

Human Mutation

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10 February 2018

volume

20

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10 February 2018

issue

5

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10 February 2018

page(s)

368-374

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10 February 2018

Characterization of MLH1 and MSH2 alternative splicing and its relevance to molecular testing of colorectal cancer susceptibility

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

The impact of L1 retrotransposons on the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

Founding mutations and Alu-mediated recombination in hereditary colon cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

An Alu-mediated 6-kb duplication in the BRCA1 gene: a new founder mutation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing: a founder mutation in the Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

Mutations of the 'minor' mismatch repair gene MSH6 in typical and atypical hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

Identification of a 3 kb Alu-mediated BRCA1 gene rearrangement in two breast/ovarian cancer families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

A 10-Mb paracentric inversion of chromosome arm 2p inactivatesMSH2 and is responsible for hereditary nonpolyposis colorectal cancer in a North-American kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

MSH2 genomic deletions are a frequent cause of HNPCC

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10138

21 January 2018

Identifiers

DOI

10.1002/HUMU.10138

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10 February 2018

1 reference

10 February 2018