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English
P1148A in fibrillin-1 is not a mutation anymore
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
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
title
P1148A in fibrillin-1 is not a mutation anymore
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
author name string
M Wang
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
K R Mathews
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
K Imaizumi
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
S Beiraghi
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
B Blumberg
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
M Scheuner
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
J M Graham
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
M Godfrey
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
publication date
1 January 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
volume
15
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
page(s)
12
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0197-12
0 references
cites work
Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-12
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation screening of complete fibrillin-1 coding sequence: report of five new mutations, including two in 8-cysteine domains
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-12
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0197-12
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0197-12
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
PubMed publication ID
8988160
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8988160
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8988160%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
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