Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q73500297)
Watch
English
A plea to search for deletion polymorphism through genome scans in populations
scientific article published on 01 October 2000
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
title
A plea to search for deletion polymorphism through genome scans in populations
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
author
Sandro Orru
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
author name string
M Siniscalco
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
R Robledo
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
L Contu
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
P Yadav
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
Q Ren
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
H Lai
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
B Roe
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
publication date
1 October 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
published in
Trends in Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
volume
16
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
issue
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
page(s)
435-437
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
cites work
The DNA sequence of human chromosome 22
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902101-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning the differences between two complex genomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902101-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative genomic analysis of tumors: detection of DNA losses and amplification
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902101-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
One-megabase sequence analysis of the human immunoglobulin lambda gene locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902101-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
V lambda and J lambda-C lambda gene segments of the human immunoglobulin lambda light chain locus are separated by 14 kb and rearrange by a deletion mechanism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902101-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Medical implications of HGP's sequence of chromosome 22
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902101-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A common molecular basis for rearrangement disorders on chromosome 22q11
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902101-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902101-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gaps in the Human Genome Project.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902101-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Population genetics--making sense out of sequence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902101-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0168-9525(00)02101-6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
PubMed publication ID
11203137
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11203137
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11203137%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
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