Molecular reclassification reveals low prevalence of germline predisposition in children with ependymoma
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource, 1 online resource.
- Language
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Englisch
- Bibliographic citation
-
Molecular reclassification reveals low prevalence of germline predisposition in children with ependymoma ; volume:11 ; number:1 ; day:12 ; month:6 ; year:2023 ; pages:1-4 ; date:12.2023
Acta Neuropathologica Communications ; 11, Heft 1 (12.6.2023), 1-4, 12.2023
- Creator
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Foss-Skiftesvik, Jon
Mathiasen, René
Overeem Hansen, Thomas van
Wadt, Karin
Schmiegelow, Kjeld
Stoltze, Ulrik Kristoffer
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s40478-023-01594-x
- URN
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urn:nbn:de:101:1-2023091913595004026034
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 14.08.2025, 11:02 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Foss-Skiftesvik, Jon
- Mathiasen, René
- Overeem Hansen, Thomas van
- Wadt, Karin
- Schmiegelow, Kjeld
- Stoltze, Ulrik Kristoffer
- SpringerLink (Online service)
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Redefining germline predisposition in children with molecularly characterized ependymoma: a population-based 20-year cohort
Genomic testing for germline predisposition to hematologic malignancies
Germline MBD4 deficiency causes a multi-tumor predisposition syndrome
Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma
Germline mutation in the RAD51B gene confers predisposition to breast cancer
A comprehensive analysis of germline predisposition to early-onset ovarian cancer
Prevalence, predisposition and prevention of type II diabetes
CDKN2A germline alterations and the relevance of genotype-phenotype associations in cancer predisposition
BUB1B monoallelic germline variants contribute to prostate cancer predisposition by triggering chromosomal instability
Germline ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
Beyond germline genetic testing - heterozygous pathogenic variants in PMS2 in two children with osteosarcoma and ependymoma
Identification of germline cancer predisposition variants in pediatric sarcoma patients from somatic tumor testing
Redefining germline predisposition in children with molecularly characterized ependymoma: a population-based 20-year cohort
Genomic testing for germline predisposition to hematologic malignancies
Germline MBD4 deficiency causes a multi-tumor predisposition syndrome
Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma
Germline mutation in the RAD51B gene confers predisposition to breast cancer
A comprehensive analysis of germline predisposition to early-onset ovarian cancer
Prevalence, predisposition and prevention of type II diabetes
CDKN2A germline alterations and the relevance of genotype-phenotype associations in cancer predisposition
BUB1B monoallelic germline variants contribute to prostate cancer predisposition by triggering chromosomal instability
Germline ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
Beyond germline genetic testing - heterozygous pathogenic variants in PMS2 in two children with osteosarcoma and ependymoma