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English
Breaking the rule of three
scientific article published in Nature
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9126731
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9126731%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
title
Human genetics. Breaking the rule of three
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9126731
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9126731%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
author name string
Mandel JL
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9126731
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9126731%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
language of work or name
English
0 references
publication date
1 April 1997
1 reference
stated in
Europe PubMed Central
PubMed ID
9126731
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9126731%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
published in
Nature
1 reference
stated in
Europe PubMed Central
PubMed ID
9126731
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9126731%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
volume
386
1 reference
stated in
Europe PubMed Central
PubMed ID
9126731
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9126731%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
page(s)
767-769
1 reference
stated in
Europe PubMed Central
PubMed ID
9126731
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9126731%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
issue
6627
1 reference
stated in
Europe PubMed Central
PubMed ID
9126731
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9126731%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
exact match
https://scigraph.springernature.com/pub.10.1038/386767a0
0 references
cites work
Trinucleotide repeats in neurogenetic disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F386767A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F386767A0
retrieved
7 January 2021
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Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F386767A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F386767A0
retrieved
7 January 2021
based on heuristic
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Molecular basis of genetic instability of triplet repeats
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F386767A0
retrieved
7 January 2021
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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F386767A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F386767A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Big, bad minisatellites
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F386767A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F386767A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F386767A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/386767A0
1 reference
stated in
Europe PubMed Central
PubMed ID
9126731
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9126731%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
Dimensions Publication ID
1052001568
0 references
PubMed ID
9126731
1 reference
stated in
Europe PubMed Central
PubMed ID
9126731
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9126731%20AND%20SRC:MED&resulttype=core&format=json
retrieved
2 November 2019
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