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English
The mutational load due to detrimental genes in man.
scientific article published in September 1960
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
1932262
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14424476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 December 2019
title
The mutational load due to detrimental genes in man
(English)
1 reference
stated in
Europe PubMed Central
PMCID
1932262
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14424476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 December 2019
author name string
MORTON NE
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1932262
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14424476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 December 2019
language of work or name
English
0 references
publication date
1 September 1960
1 reference
stated in
Europe PubMed Central
PMCID
1932262
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14424476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 December 2019
published in
American Journal of Human Genetics
1 reference
stated in
Europe PubMed Central
PMCID
1932262
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14424476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 December 2019
volume
12
1 reference
stated in
Europe PubMed Central
PMCID
1932262
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14424476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 December 2019
page(s)
348-364
1 reference
stated in
Europe PubMed Central
PMCID
1932262
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14424476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 December 2019
cites work
The incidence of consanguineous matings in Japan, with remarks on the estimation of comparative gene frequencies and the expected rate of appearance of induced recessive mutations.
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=1932262
retrieved
11 July 2018
AN ESTIMATE OF THE MUTATIONAL DAMAGE IN MAN FROM DATA ON CONSANGUINEOUS MARRIAGES
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=1932262
retrieved
11 July 2018
Formal genetics of muscular dystrophy
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=1932262
retrieved
11 July 2018
Study of somatic chromosomes from 9 mongoloid children
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=1932262
retrieved
11 July 2018
Human chromosome complements in normal somatic cells in culture.
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=1932262
retrieved
11 July 2018
Consanguineous marriages in the Chicago 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=1932262
retrieved
11 July 2018
A study of major congenital defects in Japanese infants.
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=1932262
retrieved
11 July 2018
Empirical risks in consanguineous marriages: sex ratio, malformation, and viability.
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=1932262
retrieved
11 July 2018
On the estimation of the frequency of genetic carriers.
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=1932262
retrieved
11 July 2018
Radiation dose rate and mutation frequency.
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=1932262
retrieved
24 September 2018
Comments on the inheritance of deaf mutism in Northern Ireland
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14424476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Ionizing radiation and the socially handicapped
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14424476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hereditary deaf mutism, with particular reference to Northern Ireland
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14424476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A note on deaf mutism
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14424476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Discussion of population genetics and radiation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14424476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Radiation and the sex ratio in man
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/14424476
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1932262
1 reference
stated in
Europe PubMed Central
PMCID
1932262
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14424476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 December 2019
PubMed ID
14424476
1 reference
stated in
Europe PubMed Central
PMCID
1932262
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14424476%20AND%20SRC:MED&resulttype=core&format=json
retrieved
17 December 2019
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