Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome ; volume:24 ; number:1 ; day:15 ; month:11 ; year:2024 ; pages:1-7 ; date:3.2025
Familial cancer ; 24, Heft 1 (15.11.2024), 1-7, 3.2025
- Urheber
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Brinch, Heidi Hesselø
Byrjalsen, Anna
Lohse, Zuzana
Rasmussen, Andreas Ørslev
Karstensen, John Gásdal
Kristiansen, Britta Schlott
Jelsig, Anne Marie
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1007/s10689-024-00428-6
- URN
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urn:nbn:de:101:1-2502040828526.762398068494
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:39 MESZ
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Beteiligte
- Brinch, Heidi Hesselø
- Byrjalsen, Anna
- Lohse, Zuzana
- Rasmussen, Andreas Ørslev
- Karstensen, John Gásdal
- Kristiansen, Britta Schlott
- Jelsig, Anne Marie
- SpringerLink (Online service)
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Clinically significant germline pathogenic variants are missed by tumor genomic sequencing
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Pure somatic pathogenic variation profiles for patients with serrated polyposis syndrome: a case series
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Frequency of serrated polyposis syndrome recognition by community endoscopists
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