Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: 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

Creator: Brinch, Heidi Hesselø
Byrjalsen, Anna
Lohse, Zuzana
Rasmussen, Andreas Ørslev
Karstensen, John Gásdal
Kristiansen, Britta Schlott
Jelsig, Anne Marie

Contributor: SpringerLink (Online service)

DOI: 10.1007/s10689-024-00428-6

URN: urn:nbn:de:101:1-2502040828526.762398068494

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:39 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Brinch, Heidi Hesselø
Byrjalsen, Anna
Lohse, Zuzana
Rasmussen, Andreas Ørslev
Karstensen, John Gásdal
Kristiansen, Britta Schlott
Jelsig, Anne Marie
SpringerLink (Online service)

Other Objects (12)

Serrated Polyposis Syndrome: A Literature Review

Pure somatic pathogenic variation profiles for patients with serrated polyposis syndrome: a case series

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis

Serrated polyposis syndrome: a silent killer when undetected

Frequency of serrated polyposis syndrome recognition by community endoscopists

Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

Clinically significant germline pathogenic variants are missed by tumor genomic sequencing

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

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

Evolutionary origin of germline pathogenic variants in human DNA mismatch repair genes

Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing

Genetic testing and management of prostate cancer patients with pathogenic germline variants

Serrated Polyposis Syndrome: A Literature Review

Pure somatic pathogenic variation profiles for patients with serrated polyposis syndrome: a case series

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis

Serrated polyposis syndrome: a silent killer when undetected

Frequency of serrated polyposis syndrome recognition by community endoscopists

Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

Clinically significant germline pathogenic variants are missed by tumor genomic sequencing

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

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

Evolutionary origin of germline pathogenic variants in human DNA mismatch repair genes

Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing

Genetic testing and management of prostate cancer patients with pathogenic germline variants

Serrated Polyposis Syndrome: A Literature Review

Pure somatic pathogenic variation profiles for patients with serrated polyposis syndrome: a case series

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis

Serrated polyposis syndrome: a silent killer when undetected

Frequency of serrated polyposis syndrome recognition by community endoscopists

Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

Clinically significant germline pathogenic variants are missed by tumor genomic sequencing

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

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

Evolutionary origin of germline pathogenic variants in human DNA mismatch repair genes

Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing

Genetic testing and management of prostate cancer patients with pathogenic germline variants

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Germline pathogenic variants in RNF43 in patients with and without serrated polyposis syndrome

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Serrated Polyposis Syndrome: A Literature Review

Pure somatic pathogenic variation profiles for patients with serrated polyposis syndrome: a case series

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis

Serrated polyposis syndrome: a silent killer when undetected

Frequency of serrated polyposis syndrome recognition by community endoscopists

Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

Clinically significant germline pathogenic variants are missed by tumor genomic sequencing

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

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

Evolutionary origin of germline pathogenic variants in human DNA mismatch repair genes

Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing

Genetic testing and management of prostate cancer patients with pathogenic germline variants

Serrated Polyposis Syndrome: A Literature Review

Pure somatic pathogenic variation profiles for patients with serrated polyposis syndrome: a case series

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis

Serrated polyposis syndrome: a silent killer when undetected

Frequency of serrated polyposis syndrome recognition by community endoscopists

Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

Clinically significant germline pathogenic variants are missed by tumor genomic sequencing

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

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

Evolutionary origin of germline pathogenic variants in human DNA mismatch repair genes

Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing

Genetic testing and management of prostate cancer patients with pathogenic germline variants

Serrated Polyposis Syndrome: A Literature Review

Pure somatic pathogenic variation profiles for patients with serrated polyposis syndrome: a case series

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis

Serrated polyposis syndrome: a silent killer when undetected

Frequency of serrated polyposis syndrome recognition by community endoscopists

Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort study

Clinically significant germline pathogenic variants are missed by tumor genomic sequencing

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

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

Evolutionary origin of germline pathogenic variants in human DNA mismatch repair genes

Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing

Genetic testing and management of prostate cancer patients with pathogenic germline variants

Related objects

Reset password