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Analysis of mutations in theSCH gene in schwannomas
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1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
title
Analysis of mutations in the SCH gene in schwannomas
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
author
Olivier Delattre
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
author name string
Bijlsma EK
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
Merel P
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
Bosch DA
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
Westerveld A
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
Thomas G
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
Hulsebos TJ
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
publication date
1 September 1994
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
published in
Genes, Chromosomes and Cancer
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
volume
11
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
page(s)
7-14
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
cites work
Molecular characterization of chromosome 22 deletions in schwannomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regional fine mapping of the beta crystallin genes on chromosome 22 excludes these genes as physically linked markers for neurofibromatosis type 2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assessment of chromosome 22 anomalies in neurinomas by combined karyotype and RFLP analyses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A map of 22 loci on human chromosome 22.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New markers for the neurofibromatosis-2 region generated by microdissection of chromosome 22.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of chromosome 22 alleles in human sporadic spinal schwannomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental origin of chromosome 22 loss in sporadic and NF2 neuromas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Direct assignment of the human beta B2 and beta B3 crystallin genes to 22q11.2----q12: markers for neurofibromatosis 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormalities of chromosome 22 in human brain tumors determined by combined cytogenetic and molecular genetic approaches
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frameshift mutation: determinants of specificity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effect of 5' splice site mutations on splicing of the preceding intron
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGCC.2870110103
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/10.1002%2FGCC.2870110103
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/GCC.2870110103
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
PubMed publication ID
7529050
1 reference
stated in
Europe PubMed Central
PubMed publication ID
7529050
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7529050%20AND%20SRC:MED&resulttype=core&format=json
retrieved
20 October 2019
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