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English
Linkage analysis in dominant optic atrophy
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
title
Linkage analysis in dominant optic atrophy
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
main subject
optic atrophy
1 reference
based on heuristic
inferred from title
author name string
J D Kivlin
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
E W Lovrien
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
D T Bishop
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
I H Maumenee
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
language of work or name
English
0 references
publication date
1 November 1983
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
volume
35
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
issue
6
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
page(s)
1190-1195
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
cites work
Infantile optic atrophy with dominant mode of inheritance: a clinical and genetic study of 19 Danish families
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=1685968
retrieved
13 July 2018
Sequential tests for the detection of linkage
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=1685968
retrieved
13 July 2018
Report of the committee on the genetic constitution of chromosomes 2, 3, 4, and 5
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6580816
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Linkage studies in infantile optic atrophy with a dominant mode of inheritance
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6580816
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Similarities between congenital tritan defects and dominant optic-nerve atrophy: coincidence or identity?
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6580816
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6580816
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hereditary optic atrophies in childhood
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/6580816
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMC publication ID
1685968
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
PubMed publication ID
6580816
1 reference
stated in
Europe PubMed Central
PMC publication ID
1685968
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6580816%20AND%20SRC:MED&resulttype=core&format=json
retrieved
14 October 2019
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