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Mapping of mutation causing Friedreich's ataxia to human chromosome 9
scientific article published in Nature
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
title
Mapping of mutation causing Friedreich's ataxia to human chromosome 9
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
main subject
Friedreich ataxia
1 reference
based on heuristic
inferred from title
author
Jacqui A Shaw
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
author name string
Chamberlain S
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
Rowland A
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
Wallis J
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
South S
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
Nakamura Y
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
von Gabain A
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
Farrall M
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
Williamson R
series ordinal
9
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
language of work or name
English
0 references
publication date
1 July 1988
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
published in
Nature
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
volume
334
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
page(s)
248-250
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
issue
6179
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/334248a0
0 references
cites work
Clinical Description and Roentgenologic Evaluation of Patients with Friedreich's Ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Study of Fatal Cases of Friedreich's Ataxia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A polymorphic DNA marker genetically linked to Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of cystic fibrosis locus to human chromosome 7cen–q22
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A closely linked genetic marker for cystic fibrosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exclusion of the Friedreich ataxia gene from chromosome 19
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Close linkage of alpha and beta interferons and infrequent duplication of beta interferon in humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S15).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A genetic linkage map of the human genome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The 1985 human gene map and human gene mapping in 1985
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Strategies for multilocus linkage analysis in humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Leukocyte and fibroblast interferon genes are located on human chromosome 9
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Interferon and c-ets-1 genes in the translocation (9;11)(p22;q23) in human acute monocytic leukemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Report of the Committee on the Genetic Constitution of Chromosomes 7, 8 and 9
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Friedreich's ataxia in Kathikas-Arodhes, Cyprus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F334248A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/334248A0
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
Dimensions Publication ID
1048673896
0 references
PubMed ID
2899844
1 reference
stated in
Europe PubMed Central
PubMed ID
2899844
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2899844%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 October 2019
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