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The impact of human copy number variation on gene expression
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Europe PubMed Central
PMC publication ID
4592354
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25922366%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
review article
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title
The impact of human copy number variation on gene expression
(English)
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Europe PubMed Central
PMC publication ID
4592354
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25922366%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
author
Eric R. Gamazon
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1
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Europe PubMed Central
PMC publication ID
4592354
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25922366%20AND%20SRC:MED&resulttype=core&format=json
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6 March 2020
Barbara E. Stranger
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Barbara E. Stranger
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Europe PubMed Central
PMC publication ID
4592354
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25922366%20AND%20SRC:MED&resulttype=core&format=json
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6 March 2020
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Eric R. Gamazon
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Eric R. Gamazon
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language of work or name
English
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publication date
27 April 2015
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Europe PubMed Central
PMC publication ID
4592354
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retrieved
6 March 2020
published in
Briefings in functional genomics
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stated in
Europe PubMed Central
PMC publication ID
4592354
reference URL
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retrieved
6 March 2020
volume
14
2 references
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PubMed
stated in
Europe PubMed Central
PMC publication ID
4592354
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25922366%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
issue
5
2 references
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PubMed
stated in
Europe PubMed Central
PMC publication ID
4592354
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25922366%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
page(s)
352-357
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PMC publication ID
4592354
reference URL
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retrieved
6 March 2020
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A high-resolution survey of deletion polymorphism in the human genome
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inferred from PubMed ID database lookup
Widening the spectrum of human genetic variation
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Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1
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inferred from PubMed ID database lookup
Identifiers
DOI
10.1093/BFGP/ELV017
1 reference
stated in
Europe PubMed Central
PMC publication ID
4592354
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25922366%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
PMC publication ID
4592354
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMC publication ID
4592354
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25922366%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
PubMed publication ID
25922366
2 references
stated in
PubMed
stated in
Europe PubMed Central
PMC publication ID
4592354
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25922366%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 March 2020
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