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English
Some neoplasms and some hamartomatous syndromes: genetic considerations
scientific article published on 01 October 1998
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9804200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9804200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
Some neoplasms and some hamartomatous syndromes: genetic considerations
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9804200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9804200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
author name string
M M Cohen
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9804200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9804200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
publication date
1 October 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9804200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9804200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
published in
International Journal of Oral and Maxillofacial Surgery
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9804200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9804200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
volume
27
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9804200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9804200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9804200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9804200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
page(s)
363-369
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9804200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9804200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
cites work
Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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Constitutional translocation t(4;22) (q12;q12.2) associated with neurofibromatosis type 2
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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Hereditary nonpolyposis colorectal cancer: review of clinical, molecular genetics, and counseling aspects
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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inferred from DOI database lookup
Hereditary multiple exostoses: confirmation of linkage to chromosomes 8 and 11.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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inferred from DOI database lookup
Genotype-phenotype correlations of new causative APC gene mutations in patients with familial adenomatous polyposis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
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inferred from DOI database lookup
Positional cloning of the gene for multiple endocrine neoplasia-type 1
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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inferred from DOI database lookup
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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Human Cancer Syndromes: Clues to the Origin and Nature of Cancer
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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inferred from DOI database lookup
Muir-Torre syndrome: a variant of the cancer family syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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inferred from DOI database lookup
How many epidermal nevus syndromes exist? A clinicogenetic classification
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Different karyotypic features characterize different clinico-pathologic subgroups of benign lipogenic tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
One gene—four syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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inferred from DOI database lookup
The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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inferred from DOI database lookup
Germline mutations in PTEN are present in Bannayan-Zonana syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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inferred from DOI database lookup
Localization of the gene for Cowden disease to chromosome 10q22–23
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
based on heuristic
inferred from DOI database lookup
The von Hippel-Lindau gene product inhibits vascular permeability factor/vascular endothelial growth factor expression in renal cell carcinoma by blocking protein kinase C pathways
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
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7 January 2021
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inferred from DOI database lookup
Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RET mutations in human disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial spinal neurofibromatosis: Clinical and DNA linkage analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The GDNF-RET signalling partnership
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel germline mutations in the APC gene and their phenotypic spectrum in familial adenomatous polyposis kindreds
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0901-5027%2898%2980066-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0901-5027(98)80066-0
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9804200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9804200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
PubMed publication ID
9804200
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9804200
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9804200%20AND%20SRC:MED&resulttype=core&format=json
retrieved
6 December 2019
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