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English
Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome
scientific article published on 01 January 1997
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
title
Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
main subject
fragile X syndrome
1 reference
based on heuristic
inferred from title
author name string
Wang YC
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Lin ML
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Lin SJ
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Li YC
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Li SY
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
publication date
1 January 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
published in
Human Mutation
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
volume
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
page(s)
393-399
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Identifiers
DOI
10.1002/(SICI)1098-1004(1997)10:5<393::AID-HUMU10>3.0.CO;2-V
0 references
PubMed publication ID
9375856
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9375856
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9375856%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
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