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English
The skeletal manifestations of the congenital disorders of glycosylation.
scientific article published on 06 May 2008
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
review article
1 reference
stated in
Europe PubMed Central
title
The skeletal manifestations of the congenital disorders of glycosylation
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
main subject
congenital disorder
0 references
glycosylation
1 reference
based on heuristic
inferred from title
author
David J Coman
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
author name string
M Irving
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
P Kannu
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
J Jaeken
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
R Savarirayan
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
publication date
6 May 2008
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
published in
Clinical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
volume
73
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
issue
6
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
page(s)
507-515
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
cites work
Expanding spectrum of congenital disorder of glycosylation Ig (CDG-Ig): sibs with a unique skeletal dysplasia, hypogammaglobulinemia, cardiomyopathy, genital malformations, and early lethality.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01015.X
retrieved
21 January 2018
Modulation of crystal formation by bone phosphoproteins: role of glutamic acid-rich sequences in the nucleation of hydroxyapatite by bone sialoprotein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01015.X
retrieved
21 January 2018
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01015.X
retrieved
21 January 2018
A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01015.X
retrieved
21 January 2018
The link between heparan sulfate and hereditary bone disease: finding a function for the EXT family of putative tumor suppressor proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01015.X
retrieved
21 January 2018
Identifiers
DOI
10.1111/J.1399-0004.2008.01015.X
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
PubMed ID
18462449
1 reference
stated in
Europe PubMed Central
PubMed ID
18462449
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18462449%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 January 2020
ResearchGate publication ID
5390078
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