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Mutations of the RET proto-oncogene in Hirschsprung's disease
scientific article
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instance of
scholarly article
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title
Mutations of the RET proto-oncogene in Hirschsprung's disease
(English)
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main subject
ret proto-oncogene
1 reference
stated in
GOA release 2020-03-11
posterior midgut development
1 reference
stated in
GOA release 2020-03-11
Hirschsprung's disease
1 reference
based on heuristic
inferred from title
author
Arnold Munnich
series ordinal
10
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Stanislas Lyonnet
object named as
S Lyonnet
series ordinal
2
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author name string
P Edery
series ordinal
1
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L M Mulligan
series ordinal
3
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A Pelet
series ordinal
4
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E Dow
series ordinal
5
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L Abel
series ordinal
6
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S Holder
series ordinal
7
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C Nihoul-Fékété
series ordinal
8
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B A Ponder
series ordinal
9
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language of work or name
English
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publication date
27 January 1994
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published in
Nature
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volume
367
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issue
6461
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page(s)
378-80
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cites work
Adult-Onset Hirschsprung's Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myenteric plexus in congenital megacolon; study of 11 cases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
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%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genetics of Hirschsprung's disease. Evidence for heterogeneous etiology and a study of sixty-three families.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Three-generation transmission of Hirschsprung's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MONGOLISM ASSOCIATED WITH HIRSCHSPRUNG'S DISEASE
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A case of Hirschsprung disease with a chromosome 13 microdeletion, del(13)(q32.3q33.2): potential mapping of one disease locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Association of Megacolon with Two Recessive Spotting Genes in the Mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
How sensitive is PCR-SSCP?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The human protooncogene ret: a communicative cadherin?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367378A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/367378A0
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3840761
Dimensions Publication ID
1040357518
0 references
Fatcat ID
release_euhfumf5vngq7b32e6y4voirta
0 references
OpenCitations bibliographic resource ID
3840761
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3840761
PubMed publication ID
8114939
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3840761
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