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X inactivation patterns in females with Alport's syndrome: a means of selecting against a deleterious gene?
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
title
X inactivation patterns in females with Alport's syndrome: a means of selecting against a deleterious gene?
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
main subject
Alport syndrome
1 reference
based on heuristic
inferred from title
author
David Vetrie
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
author name string
F Flinter
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
M Bobrow
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
A Harris
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
language of work or name
English
0 references
publication date
1 September 1992
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
volume
29
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
issue
9
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
page(s)
663-666
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
cites work
Isolation of a genomic clone partially encoding human hypoxanthine phosphoribosyltransferase
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=1016101
retrieved
21 June 2018
Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation
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=1016101
retrieved
21 June 2018
Localization of the gene for X-linked 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=1016101
retrieved
21 June 2018
Use of restriction fragment length polymorphisms to determine the clonal origin of human tumors
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=1016101
retrieved
21 June 2018
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=1016101
retrieved
21 June 2018
Localization of the gene for classic 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=1016101
retrieved
21 June 2018
Selection against lethal alleles in females heterozygous for incontinentia pigmenti
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=1016101
retrieved
21 June 2018
Identification of mutations in the COL4A5 collagen gene in 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=1016101
retrieved
21 June 2018
Single base mutation in α5(IV) collagen chain gene converting a conserved cysteine to serine in 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=1016101
retrieved
21 June 2018
X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease
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=1016101
retrieved
21 June 2018
Major rearrangements in the α5(IV) collagen gene in three patients with alport syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1404298
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Linkage studies in X-linked Alport's syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1404298
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Clonal analysis using recombinant DNA probes from the X-chromosome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/1404298
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.29.9.663
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
PMC publication ID
1016101
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
PubMed publication ID
1404298
1 reference
stated in
Europe PubMed Central
PMC publication ID
1016101
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1404298%20AND%20SRC:MED&resulttype=core&format=json
retrieved
15 September 2019
ResearchGate publication ID
21752013
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