(Q47739281)

5 February 2018

review article

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title

The genetics of hereditary common cancers. (English)

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5 February 2018

author

Albert de la Chapelle

series ordinal

1

object named as

de la Chapelle A

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5 February 2018

author name string

Peltomäki P

series ordinal

2

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5 February 2018

publication date

1 June 1998

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5 February 2018

Current Opinion in Genetics & Development

published in

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5 February 2018

volume

8

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5 February 2018

page(s)

298-303

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5 February 2018

issue

3

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5 February 2018

Lessons from hereditary colorectal cancer

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1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980085-3

7 January 2021

APC gene mutations and extraintestinal phenotype of familial adenomatous polyposis

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7 January 2021

Genetic identification of Mom-1, a major modifier locus affecting Min-induced intestinal neoplasia in the mouse

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7 January 2021

The secretory phospholipase A2 gene is a candidate for the Mom1 locus, a major modifier of ApcMin-induced intestinal neoplasia

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7 January 2021

Secretory phospholipase Pla2g2a confers resistance to intestinal tumorigenesis

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7 January 2021

Somatic mutations of the APC gene in colorectal tumors: mutation cluster region in the APC gene

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7 January 2021

Mutations of the APC (adenomatous polyposis coli) gene

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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

Evolution of hereditary non-polyposis colorectal cancer

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7 January 2021

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

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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

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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

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7 January 2021

DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer

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7 January 2021

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

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7 January 2021

Mutation in the mismatch repair gene Msh6 causes cancer susceptibility

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7 January 2021

Mutations predisposing to hereditary nonpolyposis colorectal cancer

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7 January 2021

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

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7 January 2021

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

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7 January 2021

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

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7 January 2021

Differential Contributions ofBRCA1andBRCA2to Early-Onset Breast Cancer

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7 January 2021

The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

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7 January 2021

BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer

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7 January 2021

Human BRCA1 inhibits growth in yeast: potential use in diagnostic testing

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7 January 2021

Detection of heterozygous truncating mutations in the BRCA1 and APC genes by using a rapid screening assay in yeast

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7 January 2021

Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search

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7 January 2021

Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980085-3

7 January 2021

Linkage analysis of 49 high-risk families does not support a common familial prostate cancer-susceptibility gene at 1q24-25.

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7 January 2021

Segregation analysis of prostate cancer in Sweden: support for dominant inheritance

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7 January 2021

The CAG repeat within the androgen receptor gene and its relationship to prostate cancer

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https://api.crossref.org/works/10.1016%2FS0959-437X%2898%2980085-3

7 January 2021

10.1016/S0959-437X(98)80085-3

Identifiers

DOI

1 reference

5 February 2018

PubMed ID

9690990

1 reference

5 February 2018