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English
Context of deletions and insertions in human coding sequences.
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1 reference
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Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
title
Context of deletions and insertions in human coding sequences
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
author
Igor B. Rogozin
series ordinal
2
1 reference
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Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
author name string
Alexey S Kondrashov
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
publication date
1 February 2004
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
published in
Human Mutation
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stated in
Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
volume
23
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
page(s)
177-185
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
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Frameshift mutation: determinants of specificity
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Use of mutation spectra analysis software.
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Somatic mutation hotspots correlate with DNA polymerase eta error spectrum.
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Mechanisms of spontaneous mutagenesis: an analysis of the spectrum of spontaneous mutation in the Escherichia coli lacI gene.
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DNA-directed mutations. Leading and lagging strand specificity
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Interspersed repeats and other mementos of transposable elements in mammalian genomes
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Frameshift mutation, microsatellites and mismatch repair
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Large majority of single-nucleotide mutations along the dystrophin gene can be explained by more than one mechanism of mutagenesis
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Mutations and polymorphisms in the human ornithine transcarbamylase gene.
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Human diallelic insertion/deletion polymorphisms
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7 January 2021
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Identifiers
DOI
10.1002/HUMU.10312
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
PubMed publication ID
14722921
1 reference
stated in
Europe PubMed Central
PubMed publication ID
14722921
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14722921%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 November 2019
ResearchGate publication ID
8920011
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