Unusual phenotypes in patients with a pathogenic germline variant in DICER1

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: 10.1007/s10689-021-00271-z

Event: Veröffentlichung

(where): Aachen

(who): Universitätsbibliothek der RWTH Aachen

(when): 2021

Creator: Venger, Kateryna
Elbracht, Miriam
Carlens, Julia
Deutz, Peter
Zeppernick, Felix
Lassay, Lisa
Kratz, Christian Peter
Zenker, Martin
Kim, Jung
Stewart, Douglas R.
Wieland, Ilse
Schultz, Kris Ann P.
Schwerk, Nicolaus
Kurth, Ingo
Kontny, Udo

DOI: 10.18154/RWTH-CONV-247049

URN: urn:nbn:de:101:1-2023021100423350438872

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:44 AM CEST

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Associated

Venger, Kateryna
Elbracht, Miriam
Carlens, Julia
Deutz, Peter
Zeppernick, Felix
Lassay, Lisa
Kratz, Christian Peter
Zenker, Martin
Kim, Jung
Stewart, Douglas R.
Wieland, Ilse
Schultz, Kris Ann P.
Schwerk, Nicolaus
Kurth, Ingo
Kontny, Udo
Universitätsbibliothek der RWTH Aachen

Time of origin

2021

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Unusual phenotypes in patients with a pathogenic germline variant in DICER1

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Other Objects (12)

Unusual phenotypes in patients with a pathogenic germline variant in DICER1

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Characterization of pathogenic germline mutations in human Protein Kinases

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Potential pathogenic germline variant reporting from tumor comprehensive genomic profiling complements classic approaches to germline testing

Myxofibrosarcoma harboring an MLH1 pathogenic germline variant associated with Muir-Torre syndrome: a case report

Germline polymorphisms as modulators of cancer phenotypes

Primary Peritoneal Carcinosarcoma in a Breast Cancer Patient Harboring a Germline BRCA2 Pathogenic Variant: Case Report

A distinct APC pathogenic germline variant identified in a southern Thai family with familial adenomatous polyposis

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COVID-19 vaccination uptake and safety profile among germline BRCA1 and BRCA2 pathogenic variant carriers in Singapore

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Attitudes toward genetic testing, family planning and preimplantation genetic testing in families with a germline CDKN2A pathogenic variant

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Potential pathogenic germline variant reporting from tumor comprehensive genomic profiling complements classic approaches to germline testing

Myxofibrosarcoma harboring an MLH1 pathogenic germline variant associated with Muir-Torre syndrome: a case report

Germline polymorphisms as modulators of cancer phenotypes

Primary Peritoneal Carcinosarcoma in a Breast Cancer Patient Harboring a Germline BRCA2 Pathogenic Variant: Case Report

A distinct APC pathogenic germline variant identified in a southern Thai family with familial adenomatous polyposis

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