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English
One gene—four syndromes
scientific article published in Nature
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7906865
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7906865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
title
Genetics. One gene--four syndromes
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7906865
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7906865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
author
Veronica van Heyningen
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7906865
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7906865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
language of work or name
English
0 references
publication date
1 January 1994
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7906865
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7906865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
published in
Nature
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7906865
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7906865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
volume
367
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7906865
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7906865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
issue
6461
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7906865
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7906865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
page(s)
319-320
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7906865
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7906865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/367319a0
0 references
cites work
A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367319A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367319A0
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%2F367319A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367319A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PTC is a novel rearranged form of the ret proto-oncogene and is frequently detected in vivo in human thyroid papillary carcinomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367319A0
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%2F367319A0
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%2F367319A0
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%2F367319A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F367319A0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/367319A0
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7906865
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7906865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
Dimensions Publication ID
1047636790
0 references
PubMed publication ID
7906865
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7906865
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7906865%20AND%20SRC:MED&resulttype=core&format=json
retrieved
28 October 2019
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