Molecular tumor testing in patients with Lynch-like syndrome reveals a de novo mosaic variant of a mismatch repair gene transmitted to offspring (Q97550251)

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scientific article published on 16 July 2020

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English	Molecular tumor testing in patients with Lynch-like syndrome reveals a de novo mosaic variant of a mismatch repair gene transmitted to offspring	scientific article published on 16 July 2020

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32678338%20AND%20SRC:MED&resulttype=core&format=json

20 July 2020

Molecular tumor testing in patients with Lynch-like syndrome reveals a de novo mosaic variant of a mismatch repair gene transmitted to offspring (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32678338%20AND%20SRC:MED&resulttype=core&format=json

20 July 2020

DNA mismatch repair

1 reference

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author name string

Erell Guillerm

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32678338%20AND%20SRC:MED&resulttype=core&format=json

20 July 2020

Magali Svrcek

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32678338%20AND%20SRC:MED&resulttype=core&format=json

20 July 2020

Armelle Bardier-Dupas

3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32678338%20AND%20SRC:MED&resulttype=core&format=json

20 July 2020

Noémie Basset

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32678338%20AND%20SRC:MED&resulttype=core&format=json

20 July 2020

Florence Coulet

5

1 reference

Europe PubMed Central

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20 July 2020

Chrystelle Colas

6

1 reference

Europe PubMed Central

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20 July 2020

publication date

16 July 2020

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Europe PubMed Central

PubMed publication ID

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20 July 2020

European Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32678338%20AND%20SRC:MED&resulttype=core&format=json

20 July 2020

Differentiating Lynch-like from Lynch syndrome

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The mystery of mismatch repair deficiency: lynch or lynch-like?

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics and Genetic Testing in Hereditary Colorectal Cancer

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Risk of cancer in cases of suspected lynch syndrome without germline mutation.

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic aberrations of mismatch repair genes as a cause of microsatellite-unstable cancers

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis.

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic mosaicism and double somatic hits can lead to MSI colorectal tumors

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic mutations in MLH1 and MSH2 are a frequent cause of mismatch-repair deficiency in Lynch syndrome-like tumors

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Biallelic MUTYH mutations can mimic Lynch syndrome

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions.

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of germline MUTYH mutations among Lynch-like syndrome patients

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline variants in POLE are associated with early onset mismatch repair deficient colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatic mosaicism in a patient with Lynch syndrome

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Determining the frequency of de novo germline mutations in DNA mismatch repair genes

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Mosaicism and prenatal diagnosis options: insights from retinoblastoma

1 reference

https://api.crossref.org/works/10.1038%2FS41431-020-0689-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/S41431-020-0689-6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32678338%20AND%20SRC:MED&resulttype=core&format=json

20 July 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:32678338%20AND%20SRC:MED&resulttype=core&format=json

20 July 2020

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