(Q44169977)

30 November 2017

title

Familial microsatellite-stable non-polyposis colorectal cancer: incidence and characteristics in a clinic-based population (English)

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30 November 2017

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V Rovella

1

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Emanuela Lucci Cordisco

object named as

E Lucci-Cordisco

6

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Maurizio Genuardi

object named as

M Genuardi

9

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author name string

S Carrara

2

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30 November 2017

S C Crucitti

3

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30 November 2017

C Coco

4

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30 November 2017

P Magistrelli

5

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30 November 2017

M Anti

7

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30 November 2017

G Neri

8

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30 November 2017

language of work or name

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1 June 2001

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30 November 2017

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30 November 2017

volume

12

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30 November 2017

issue

6

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30 November 2017

page(s)

813-818

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Screening and genetic counselling for relatives of patients with colorectal cancer in a family cancer clinic

30 November 2017

cites work

1 reference

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7 January 2021

Cancer risk in relatives of patients with common colorectal cancer.

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A Prospective Study of Family History and the Risk of Colorectal Cancer

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7 January 2021

Identification and characterization of the familial adenomatous polyposis coli gene

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7 January 2021

Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives.

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7 January 2021

Clues to the pathogenesis of familial colorectal cancer

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7 January 2021

Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer

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7 January 2021

Genetic testing is important in families with a history suggestive of hereditary non-polyposis colorectal cancer even if the Amsterdam criteria are not fulfilled

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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

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7 January 2021

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

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7 January 2021

Familial endometrial cancer in female carriers of MSH6 germline mutations

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7 January 2021

Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations.

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7 January 2021

Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease

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7 January 2021

Microsatellite instability-a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer

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7 January 2021

Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.

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7 January 2021

The APCI1307K allele and cancer risk in a community-based study of Ashkenazi Jews

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7 January 2021

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

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7 January 2021

HNPCC associated with germline mutation in the TGF-beta type II receptor gene.

1 reference

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7 January 2021

Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability

1 reference

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7 January 2021

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

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7 January 2021

Epigenetic phenotypes distinguish microsatellite-stable and -unstable colorectal cancers

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7 January 2021

Microsatellite instability in early onset and familial colorectal cancer.

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7 January 2021

The value of microsatellite instability in the detection of HNPCC families and of sporadic colorectal cancers with special biological features: an investigation on a series of 100 consecutive cases

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1011182025556

7 January 2021

Population-based molecular detection of hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1011182025556

7 January 2021

Mutations in the SMAD4/DPC4 gene in juvenile polyposis

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1011182025556

7 January 2021

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1023%2FA%3A1011182025556

7 January 2021

Identifiers

DOI

10.1023/A:1011182025556

1 reference

30 November 2017

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