(Q51496771)

5 April 2018

title

Identification of new cases of early-onset colorectal cancer with an MLH1 epimutation in an ethnically diverse South African cohort. (English)

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6

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author name string

M P Hitchins

1

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S E Owens

2

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C-T Kwok

3

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G Godsmark

4

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U F Algar

5

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publication date

4 May 2011

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5 April 2018

published in

Clinical Genetics

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volume

80

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issue

5

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page(s)

428-434

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Lynch syndrome: history and current status

cites work

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Constitutional (germline) MLH1 epimutation as an aetiological mechanism for hereditary non-polyposis colorectal cancer

21 January 2018

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Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.

21 January 2018

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Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome

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Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study

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Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome.

21 January 2018

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Extensive but hemiallelic methylation of the hMLH1 promoter region in early-onset sporadic colon cancers with microsatellite instability

21 January 2018

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Germline epimutation of MLH1 in individuals with multiple cancers

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MLH1 Germline Epimutations as a Factor in Hereditary Nonpolyposis Colorectal Cancer

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Inheritance of a Cancer-AssociatedMLH1Germ-Line Epimutation

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MLH1 promoter germline-methylation in selected probands of Chinese hereditary non-polyposis colorectal cancer families

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Early onset MSI-H colon cancer with MLH1 promoter methylation, is there a genetic predisposition?

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De novo constitutional MLH1 epimutations confer early-onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

Identifiers

DOI

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5 April 2018

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5 April 2018