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English
Population genetic studies of retinitis pigmentosa.
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
title
Population genetic studies of retinitis pigmentosa
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
main subject
population genetics
0 references
author name string
J A Boughman
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
P M Conneally
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
W E Nance
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
language of work or name
English
0 references
publication date
1 March 1980
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
volume
32
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
page(s)
223-235
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
cites work
The mutational load due to detrimental genes in man
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=1686021
retrieved
13 July 2018
RECESSIVE GENES IN SEVERE MENTAL DEFECT
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=1686021
retrieved
13 July 2018
ESTIMATION OF PREVALENCE UNDER INCOMPLETE SELECTION.
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=1686021
retrieved
13 July 2018
Genetic and epidemiological investigations on pigmentary degeneration of the retina and allied disorders in Switzerland
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=1686021
retrieved
13 July 2018
A General Model for the Genetic Analysis of Pedigree Data
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=1686021
retrieved
13 July 2018
Symposium: pigmentary retinopathy summing-up
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=1686021
retrieved
13 July 2018
Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1686021
retrieved
13 July 2018
Sex-linked recessive congenital deafness and the excess of males in profound childhood deafness
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7386458
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Rod Responses in Retinitis Pigmentosa, Dominantly Inherited
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7386458
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hereditary aspects of pigmentary retinopathy
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7386458
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Primary retinal pigmentary degeneration
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7386458
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Pedigree analysis to determine the mode of inheritance in a family with retinitis pigmentosa
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7386458
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Retinal degeneration in cats fed casein. I. Taurine deficiency
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7386458
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Electrophysiological abnormalities in pigmentary degenerations of the retina. Assessment of value and basis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7386458
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1686021
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
PubMed ID
7386458
1 reference
stated in
Europe PubMed Central
PMCID
1686021
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7386458%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 October 2019
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