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English
A common SNP haplotype provides molecular proof of a founder effect of Huntington disease linking two South African populations.
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scholarly article
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stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
title
A common SNP haplotype provides molecular proof of a founder effect of Huntington disease linking two South African populations
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
main subject
Huntington's disease
0 references
South Africa
0 references
founder effect
1 reference
based on heuristic
inferred from title
author
Janine Scholefield
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
author name string
Jacquie Greenberg
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
publication date
28 February 2007
1 reference
stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
published in
European Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
volume
15
1 reference
stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
page(s)
590-595
1 reference
stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
exact match
https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201796
0 references
cites work
Diagnosis of Huntington Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A single allele from the polymorphic CCG rich sequence immediately 3' to the unstable CAG trinucleotide in the IT15 cDNA shows almost complete disequilibrium with Huntington's disease chromosomes in the Scottish population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage disequilibrium between the expanded (CAG)n repeat and an allele of the adjacent (CCG)n repeat in Huntington's disease patients of Greek origin.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic linkage between Huntington disease and the D4S10 locus in South African families: further evidence against non-allelic heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allelic discrimination by denaturing high-performance liquid chromatography
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Faster haplotype frequency estimation using unrelated subjects.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201796
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/SJ.EJHG.5201796
1 reference
stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
Dimensions Publication ID
1048784142
0 references
PubMed ID
17327878
1 reference
stated in
Europe PubMed Central
PubMed ID
17327878
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17327878%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 December 2019
ResearchGate publication ID
6478432
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