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Clinical utility gene card for: Alport syndrome
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
title
Clinical utility gene card for: Alport syndrome
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
main subject
Alport syndrome
1 reference
based on heuristic
inferred from title
author
Jens M Hertz
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
Helen Storey
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
author name string
Mads Thomassen
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
Frances Flinter
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
language of work or name
English
0 references
publication date
14 December 2011
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
published in
European Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
volume
20
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
issue
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
cites work
The value of clinical criteria in identifying patients with X-linked Alport syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355248
retrieved
7 April 2017
X-linked inheritance of Alport syndrome: family P revisited
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355248
retrieved
27 September 2017
Genetics of classic Alport's syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355248
retrieved
27 September 2017
Alport's syndrome in 78 patients: epidemiological and clinical study.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355248
retrieved
30 May 2018
MLPA and cDNA analysis improves COL4A5 mutation detection in X-linked Alport syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FEJHG.2011.237
retrieved
21 January 2018
Alport syndrome in southern Sweden.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355248
retrieved
28 November 2018
X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3355248
retrieved
28 November 2018
Identifiers
DOI
10.1038/EJHG.2011.237
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
Dimensions Publication ID
1049597889
0 references
PMC publication ID
3355248
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
PubMed publication ID
22166944
1 reference
stated in
Europe PubMed Central
PMC publication ID
3355248
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22166944%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 January 2020
ResearchGate publication ID
51876069
0 references
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