Location via proxy:
[ UP ]
[Report a bug]
[Manage cookies]
No cookies
No scripts
No ads
No referrer
Show this form
Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q94465012)
Watch
English
A high-resolution survey of deletion polymorphism in the human genome
No description defined
In more languages
default for all languages
No label defined
No description defined
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
title
A high-resolution survey of deletion polymorphism in the human genome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
author
Dan Andrews
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
Jonathan K. Pritchard
series ordinal
5
object named as
Jonathan K Pritchard
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
author name string
Donald F Conrad
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
Nigel P Carter
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
Matthew E Hurles
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
publication date
4 December 2005
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
volume
38
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
page(s)
75-81
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
cites work
Large-scale copy number polymorphism in the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
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%2FNG1697
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%2FNG1697
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%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The International HapMap Project
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Contiguous gene syndromes: a component of recognizable syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Presence of large deletions in kindreds with autism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutational equilibrium model of genome size evolution
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
When less is more: gene loss as an engine of evolutionary change
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional Identification of Microdeletions with Genetic Markers
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human diallelic insertion/deletion polymorphisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
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%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
As normal as normal can be?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
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%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparison of the genomes of human and mouse lays the foundation of genome zoology
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
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%2FNG1697
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%2FNG1697
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%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1697
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG1697
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
PubMed publication ID
16327808
1 reference
stated in
Europe PubMed Central
PubMed publication ID
16327808
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16327808%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 May 2020
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
