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English
Somatic instability of the myotonic dystrophy (CTG)n repeat during human fetal development
scientific article published on 01 June 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
title
Somatic instability of the myotonic dystrophy (CTG)n repeat during human fetal development
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
main subject
myotonic dystrophy
1 reference
based on heuristic
inferred from title
author name string
L Martorell
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
K Johnson
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
C A Boucher
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
M Baiget
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
publication date
1 June 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
published in
Human Molecular Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
volume
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
issue
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
page(s)
877-880
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
Identifiers
DOI
10.1093/HMG/6.6.877
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
PubMed publication ID
9175733
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9175733
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9175733%20AND%20SRC:MED&resulttype=core&format=json
retrieved
3 November 2019
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