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English
I1307K APC and hMLH1 mutations in a non-Jewish family with hereditary non-polyposis colorectal cancer
scientific article published on 01 October 1998
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
title
I1307K APC and hMLH1 mutations in a non-Jewish family with hereditary non-polyposis colorectal cancer
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
main subject
colorectal cancer
1 reference
based on heuristic
inferred from title
colorectal carcinoma
1 reference
based on heuristic
inferred from title
author
William David Foulkes
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
author name string
Z Q Yuan
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
L Kasprzak
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
P H Gordon
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
L Pinsky
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
publication date
1 October 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
volume
54
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
page(s)
368-370
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
cites work
Lessons from hereditary colorectal cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1998.5440421.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1998.5440421.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1998.5440421.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1998.5440421.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1034%2FJ.1399-0004.1998.5440421.X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1034/J.1399-0004.1998.5440421.X
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
PubMed publication ID
9831355
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9831355
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9831355%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
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