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English
Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations.
scientific article published on 20 January 2008
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
title
Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations
(English)
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
main subject
homozygosity
1 reference
based on heuristic
inferred from title
author
David Curtis
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
Jo Knight
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
author name string
A E Vine
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
language of work or name
English
0 references
publication date
20 January 2008
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
published in
Annals of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
volume
72
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
issue
Pt 2
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
page(s)
261-278
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
cites work
Extended homozygosity is not usually due to cytogenetic abnormality
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343471
retrieved
9 September 2017
GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343471
retrieved
9 September 2017
A comparison of phasing algorithms for trios and unrelated individuals
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343471
retrieved
9 September 2017
A haplotype map of the human genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343471
retrieved
9 September 2017
Genomewide distribution of high-frequency, completely mismatching SNP haplotype pairs observed to be common across human populations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343471
retrieved
9 September 2017
Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343471
retrieved
9 September 2017
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343471
retrieved
30 September 2017
Mapping trait loci by use of inferred ancestral recombination graphs
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343471
retrieved
30 September 2017
Extended tracts of homozygosity in outbred human populations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2343471
retrieved
20 September 2018
Identifiers
DOI
10.1111/J.1469-1809.2007.00411.X
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
PMCID
2343471
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
PubMed ID
18205893
1 reference
stated in
Europe PubMed Central
PMCID
2343471
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18205893%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 January 2020
ResearchGate publication ID
5645515
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