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English
Common deletions and SNPs are in linkage disequilibrium in the human genome
scientific article published on 04 December 2005
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
title
Common deletions and SNPs are in linkage disequilibrium in the human genome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
main subject
disequilibrium
1 reference
based on heuristic
inferred from title
linkage disequilibrium
1 reference
based on heuristic
inferred from title
author
David A Hinds
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
Kelly A. Frazer
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
author name string
Andrew P Kloek
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
Michael Jen
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
Xiyin Chen
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
language of work or name
English
0 references
publication date
4 December 2005
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
volume
38
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
page(s)
82-85
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
cites work
Frequency and predictive value of 22q11 deletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
21 January 2018
Fine-scale structural variation of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Segmental duplications and copy-number variation in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A common inversion under selection in Europeans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
alpha-Synuclein locus triplication causes Parkinson's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Large-scale copy number polymorphism in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Detection of large-scale variation in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of single-nucleotide polymorphisms in coding regions of human genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A population study of chromosome 22q11 deletions in infancy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of 22q11 microdeletion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel α-globin gene arrangement in man
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The chromosomal arrangement of human alpha-like globin genes: sequence homology and alpha-globin gene deletions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular mechanisms for genomic disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A high-resolution survey of deletion polymorphism in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Common deletion polymorphisms in the human genome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recent segmental duplications in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Whole-genome patterns of common DNA variation in three human populations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1695
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG1695
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
PubMed publication ID
16327809
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327809
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327809%20AND%20SRC:MED&resulttype=core&format=json
retrieved
10 January 2020
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