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English
Positional cloning moves from perditional to traditional
scientific article published on 01 April 1995
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Europe PubMed Central
PubMed publication ID
7795639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
title
Positional cloning moves from perditional to traditional
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7795639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
author
Francis Collins
series ordinal
1
object named as
Collins FS
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7795639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
publication date
1 April 1995
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7795639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7795639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
volume
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7795639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7795639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
page(s)
347-350
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7795639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
cites work
Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning: let's not call it reverse anymore
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The rise and fall of positional cloning?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Trinucleotide repeat expansions and human genetic disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Location on chromosome 15 of the gene defect causing Marfan syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of the RET proto-oncogene in Hirschsprung's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic dissection of complex traits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A genome-wide search for human type 1 diabetes susceptibility genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Light-generated oligonucleotide arrays for rapid DNA sequence analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0495-347
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0495-347
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7795639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
PubMed publication ID
7795639
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7795639
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7795639%20AND%20SRC:MED&resulttype=core&format=json
retrieved
26 October 2019
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