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MSH2 genomic deletions are a frequent cause of HNPCC
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
title
MSH2 genomic deletions are a frequent cause of HNPCC
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
main subject
Lynch syndrome
1 reference
based on heuristic
inferred from title
author
Juul T Wijnen
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Hans Vasen
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Dick Lindhout
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Riccardo Fodde
series ordinal
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Marjolein van der Klift
series ordinal
2
object named as
van der Klift H
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author name string
Khan PM
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Menko F
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Tops C
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Meijers Heijboer H
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Møller P
series ordinal
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
language of work or name
English
0 references
publication date
1 December 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
volume
20
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
page(s)
326-328
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
exact match
https://scigraph.springernature.com/pub.10.1038/3795
0 references
cites work
Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of a mutL homolog in hereditary colon cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Founding mutations and Alu-mediated recombination in hereditary colon cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Monoallelic mutation analysis (MAMA) for identifying germline mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3795
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/3795
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
Dimensions Publication ID
1011193593
0 references
PubMed publication ID
9843200
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9843200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
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