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Hirschsprung's disease: dissecting complexity in a pathogenetic network
scientific article published on 01 April 2002
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11955531
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11955531%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
title
Hirschsprung's disease: dissecting complexity in a pathogenetic network
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11955531
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11955531%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
main subject
Hirschsprung's disease
1 reference
based on heuristic
inferred from title
author name string
Edward R B McCabe
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11955531
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11955531%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
language of work or name
English
0 references
publication date
1 April 2002
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11955531
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11955531%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
published in
The Lancet
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11955531
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11955531%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
volume
359
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11955531
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11955531%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
issue
9313
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11955531
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11955531%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
page(s)
1169-1170
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11955531
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11955531%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
cites work
Monogenic traits are not simple: lessons from phenylketonuria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2908249-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2908249-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Modifier genes convert "simple" Mendelian disorders to complex traits
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2908249-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Consequences of complexity within biological networks: robustness and health, or vulnerability and disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2908249-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2908249-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathways
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2908249-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterozygosity: an expanding role in proteomics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2908249-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hirschsprung's disease in a family with multiple endocrine neoplasia type 2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2908249-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple endocrine neoplasia type II B with symptoms suggesting Hirschsprung's disease: a case report
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0140-6736%2802%2908249-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0140-6736(02)08249-1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11955531
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11955531%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
PubMed publication ID
11955531
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11955531
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11955531%20AND%20SRC:MED&resulttype=core&format=json
retrieved
9 December 2019
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