Validation structures for sequence variants of uncertain significance in hereditary cancer.
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| Title: | Validation structures for sequence variants of uncertain significance in hereditary cancer. |
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| Authors: | Lucas MC; MGZ - Medical Genetics Center, Munich, Germany. morghan.lucas@mgz-muenchen.de.; Medizinische Klinik und Poliklinik IV - Campus Innenstadt, Klinikum der Universität München, Munich, Germany. morghan.lucas@mgz-muenchen.de., Keßler T; MGZ - Medical Genetics Center, Munich, Germany., Benet-Pagès A; MGZ - Medical Genetics Center, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, German Research Centre for Environmental Health, Munich, Germany., Holinski-Feder E; MGZ - Medical Genetics Center, Munich, Germany.; Medizinische Klinik und Poliklinik IV - Campus Innenstadt, Klinikum der Universität München, Munich, Germany.; Genturis European Reference Network (ERN) Genetic Tumor Risk (GENTURIS), Nijmegen, Netherlands., Laner A; MGZ - Medical Genetics Center, Munich, Germany., Klink B; MGZ - Medical Genetics Center, Munich, Germany. barbara.klink@mgz-muenchen.de.; Medizinische Klinik und Poliklinik IV - Campus Innenstadt, Klinikum der Universität München, Munich, Germany. barbara.klink@mgz-muenchen.de.; Genturis European Reference Network (ERN) Genetic Tumor Risk (GENTURIS), Nijmegen, Netherlands. barbara.klink@mgz-muenchen.de. |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2026 Mar 10. Date of Electronic Publication: 2026 Mar 10. |
| Publication Type: | Journal Article; Review |
| Journal Info: | Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41807735 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Validation structures for sequence variants of uncertain significance in hereditary cancer. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Lucas+MC%22">Lucas MC</searchLink>; MGZ - Medical Genetics Center, Munich, Germany. morghan.lucas@mgz-muenchen.de.; Medizinische Klinik und Poliklinik IV - Campus Innenstadt, Klinikum der Universität München, Munich, Germany. morghan.lucas@mgz-muenchen.de.<br /><searchLink fieldCode="AU" term="%22Keßler+T%22">Keßler T</searchLink>; MGZ - Medical Genetics Center, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Benet-Pagès+A%22">Benet-Pagès A</searchLink>; MGZ - Medical Genetics Center, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, German Research Centre for Environmental Health, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Holinski-Feder+E%22">Holinski-Feder E</searchLink>; MGZ - Medical Genetics Center, Munich, Germany.; Medizinische Klinik und Poliklinik IV - Campus Innenstadt, Klinikum der Universität München, Munich, Germany.; Genturis European Reference Network (ERN) Genetic Tumor Risk (GENTURIS), Nijmegen, Netherlands.<br /><searchLink fieldCode="AU" term="%22Laner+A%22">Laner A</searchLink>; MGZ - Medical Genetics Center, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Klink+B%22">Klink B</searchLink>; MGZ - Medical Genetics Center, Munich, Germany. barbara.klink@mgz-muenchen.de.; Medizinische Klinik und Poliklinik IV - Campus Innenstadt, Klinikum der Universität München, Munich, Germany. barbara.klink@mgz-muenchen.de.; Genturis European Reference Network (ERN) Genetic Tumor Risk (GENTURIS), Nijmegen, Netherlands. barbara.klink@mgz-muenchen.de. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229302235%22">European journal of human genetics : EJHG</searchLink> [Eur J Hum Genet] 2026 Mar 10. <i>Date of Electronic Publication: </i>2026 Mar 10. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Review – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Publishing+Group%22">Nature Publishing Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9302235 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1476-5438 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210184813%22">10184813 </searchLink><i>NLM ISO Abbreviation: </i>Eur J Hum Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41807735 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/s41431-026-02073-2 Languages: – Code: eng Text: English Titles: – TitleFull: Validation structures for sequence variants of uncertain significance in hereditary cancer. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Lucas MC – PersonEntity: Name: NameFull: Keßler T – PersonEntity: Name: NameFull: Benet-Pagès A – PersonEntity: Name: NameFull: Holinski-Feder E – PersonEntity: Name: NameFull: Laner A – PersonEntity: Name: NameFull: Klink B IsPartOfRelationships: – BibEntity: Dates: – D: 10 M: 03 Text: 2026 Mar 10 Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1476-5438 Titles: – TitleFull: European journal of human genetics : EJHG Type: main |
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