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English
Homozygosity mapping: familiarity breeds debility
scientific article published on 01 October 1993
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8252033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
title
Homozygosity mapping: familiarity breeds debility
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8252033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
main subject
homozygosity
1 reference
based on heuristic
inferred from title
author name string
Farrall M
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8252033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
publication date
1 October 1993
1 reference
stated in
Europe PubMed Central
PubMed ID
8252033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
8252033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
volume
5
1 reference
stated in
Europe PubMed Central
PubMed ID
8252033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
page(s)
107-108
1 reference
stated in
Europe PubMed Central
PubMed ID
8252033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
8252033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng1093-107
0 references
cites work
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1093-107
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1093-107
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1093-107
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1093-107
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic homogeneity between acute and chronic forms of spinal muscular atrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1093-107
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic linkage of Werner's syndrome to five markers on chromosome 8
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1093-107
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1093-107
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1093-107
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The association of characters as a result of inbreeding and linkage
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1093-107
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Efficient methods for computing linkage likelihoods of recessive diseases in inbred pedigrees
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1093-107
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG1093-107
1 reference
stated in
Europe PubMed Central
PubMed ID
8252033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
PubMed ID
8252033
1 reference
stated in
Europe PubMed Central
PubMed ID
8252033
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8252033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
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