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English
Widening the spectrum of human genetic variation
scientific article published on 01 January 2006
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
16380720
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16380720%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
title
Widening the spectrum of human genetic variation
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
16380720
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16380720%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
author name string
Evan E Eichler
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16380720
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16380720%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
publication date
1 January 2006
1 reference
stated in
Europe PubMed Central
PubMed ID
16380720
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16380720%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
16380720
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16380720%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
volume
38
1 reference
stated in
Europe PubMed Central
PubMed ID
16380720
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16380720%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
page(s)
9-11
1 reference
stated in
Europe PubMed Central
PubMed ID
16380720
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16380720%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16380720
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16380720%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
exact match
https://scigraph.springernature.com/pub.10.1038/ng0106-9
0 references
cites work
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%2FNG0106-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A haplotype map of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0106-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Common deletions and SNPs are in linkage disequilibrium in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0106-9
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%2FNG0106-9
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%2FNG0106-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fine-scale structural variation of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0106-9
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%2FNG0106-9
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%2FNG0106-9
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%2FNG0106-9
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%2FNG0106-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic disorders: genome architecture results in susceptibility to DNA rearrangements causing common human traits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0106-9
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%2FNG0106-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Complex SNP-related sequence variation in segmental genome duplications.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0106-9
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%2FNG0106-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0106-9
1 reference
stated in
Europe PubMed Central
PubMed ID
16380720
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16380720%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
PubMed ID
16380720
1 reference
stated in
Europe PubMed Central
PubMed ID
16380720
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16380720%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 January 2020
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