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English
Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency.
scientific article published on September 1988
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
title
Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
author name string
G Rumsby
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
A H Fielder
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
W M Hague
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
J W Honour
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
language of work or name
English
0 references
publication date
1 September 1988
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
volume
25
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
issue
9
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
page(s)
596-599
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
cites work
HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation
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=1051536
retrieved
27 May 2018
Polymorphic DNA region adjacent to the 5' end of the human insulin gene
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=1051536
retrieved
27 May 2018
Structure and organization of theC4genes
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=1051536
retrieved
27 May 2018
Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia
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=1051536
retrieved
27 May 2018
P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia
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=1051536
retrieved
27 May 2018
Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia
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=1051536
retrieved
27 May 2018
Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants
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=1051536
retrieved
27 May 2018
Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region
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=1051536
retrieved
27 May 2018
Detection of specific sequences among DNA fragments separated by gel electrophoresis
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=1051536
retrieved
27 May 2018
Statement on the nomenclature of human C4 allotypes.
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=1051536
retrieved
16 August 2018
Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3263505
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.25.9.596
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
PMCID
1051536
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
PubMed ID
3263505
1 reference
stated in
Europe PubMed Central
PMCID
1051536
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3263505%20AND%20SRC:MED&resulttype=core&format=json
retrieved
21 September 2019
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