Overview on WHO-HAEM5 and the diagnostic relevance of genetic alterations for the classification

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Overview on WHO-HAEM5 and the diagnostic relevance of genetic alterations for the classification ; volume:36 ; number:1 ; year:2024 ; pages:3-11 ; extent:9
Medizinische Genetik ; 36, Heft 1 (2024), 3-11 (gesamt 9)

Creator: Haferlach, Claudia
Haferlach, Torsten
Hörst, Katharina
Kühn, Constanze
Ott, German
Siebert, Reiner

DOI: 10.1515/medgen-2024-2008

URN: urn:nbn:de:101:1-2024030613535354618302

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

Last update: 14.08.2025, 10:50 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

Haferlach, Claudia
Haferlach, Torsten
Hörst, Katharina
Kühn, Constanze
Ott, German
Siebert, Reiner

Other Objects (12)

Genetic alterations in the classification of tumors of the haematopoietic system: From guiding diagnosis to instructing treatment in leukaemias and lymphomas

Appraisal of current technologies for the study of genetic alterations in hematologic malignancies with a focus on chromosome analysis and structural variants

Genetic alterations in chronic lymphocytic leukemia and plasma cell neoplasms – a practical guide to WHO HAEM5

Pränataldiagnostik

Seltene Tumordispositionssyndrome

Genetic alterations in mature B- and T-cell lymphomas – a practical guide to WHO-HAEM5

Impact of a faulty germinal center reaction on the pathogenesis of primary diffuse large B cell lymphoma of the central nervous system

Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B cell lymphomas

SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome

Primary adenocarcinoma of the thymus: an immunohistochemical and molecular study with review of the literature

Current molecular and clinical landscape of ATRT: the link to future therapies

No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control

Genetic alterations in the classification of tumors of the haematopoietic system: From guiding diagnosis to instructing treatment in leukaemias and lymphomas

Appraisal of current technologies for the study of genetic alterations in hematologic malignancies with a focus on chromosome analysis and structural variants

Genetic alterations in chronic lymphocytic leukemia and plasma cell neoplasms – a practical guide to WHO HAEM5

Pränataldiagnostik

Seltene Tumordispositionssyndrome

Genetic alterations in mature B- and T-cell lymphomas – a practical guide to WHO-HAEM5

Impact of a faulty germinal center reaction on the pathogenesis of primary diffuse large B cell lymphoma of the central nervous system

Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B cell lymphomas

SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome

Primary adenocarcinoma of the thymus: an immunohistochemical and molecular study with review of the literature

Current molecular and clinical landscape of ATRT: the link to future therapies

No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control

Genetic alterations in the classification of tumors of the haematopoietic system: From guiding diagnosis to instructing treatment in leukaemias and lymphomas

Appraisal of current technologies for the study of genetic alterations in hematologic malignancies with a focus on chromosome analysis and structural variants

Genetic alterations in chronic lymphocytic leukemia and plasma cell neoplasms – a practical guide to WHO HAEM5

Pränataldiagnostik

Seltene Tumordispositionssyndrome

Genetic alterations in mature B- and T-cell lymphomas – a practical guide to WHO-HAEM5

Impact of a faulty germinal center reaction on the pathogenesis of primary diffuse large B cell lymphoma of the central nervous system

Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B cell lymphomas

SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome

Primary adenocarcinoma of the thymus: an immunohistochemical and molecular study with review of the literature

Current molecular and clinical landscape of ATRT: the link to future therapies

No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control

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.

Overview on WHO-HAEM5 and the diagnostic relevance of genetic alterations for the classification

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Genetic alterations in the classification of tumors of the haematopoietic system: From guiding diagnosis to instructing treatment in leukaemias and lymphomas

Appraisal of current technologies for the study of genetic alterations in hematologic malignancies with a focus on chromosome analysis and structural variants

Genetic alterations in chronic lymphocytic leukemia and plasma cell neoplasms – a practical guide to WHO HAEM5

Pränataldiagnostik

Seltene Tumordispositionssyndrome

Genetic alterations in mature B- and T-cell lymphomas – a practical guide to WHO-HAEM5

Impact of a faulty germinal center reaction on the pathogenesis of primary diffuse large B cell lymphoma of the central nervous system

Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B cell lymphomas

SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome

Primary adenocarcinoma of the thymus: an immunohistochemical and molecular study with review of the literature

Current molecular and clinical landscape of ATRT: the link to future therapies

No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control

Genetic alterations in the classification of tumors of the haematopoietic system: From guiding diagnosis to instructing treatment in leukaemias and lymphomas

Appraisal of current technologies for the study of genetic alterations in hematologic malignancies with a focus on chromosome analysis and structural variants

Genetic alterations in chronic lymphocytic leukemia and plasma cell neoplasms – a practical guide to WHO HAEM5

Pränataldiagnostik

Seltene Tumordispositionssyndrome

Genetic alterations in mature B- and T-cell lymphomas – a practical guide to WHO-HAEM5

Impact of a faulty germinal center reaction on the pathogenesis of primary diffuse large B cell lymphoma of the central nervous system

Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B cell lymphomas

SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome

Primary adenocarcinoma of the thymus: an immunohistochemical and molecular study with review of the literature

Current molecular and clinical landscape of ATRT: the link to future therapies

No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control

Genetic alterations in the classification of tumors of the haematopoietic system: From guiding diagnosis to instructing treatment in leukaemias and lymphomas

Appraisal of current technologies for the study of genetic alterations in hematologic malignancies with a focus on chromosome analysis and structural variants

Genetic alterations in chronic lymphocytic leukemia and plasma cell neoplasms – a practical guide to WHO HAEM5

Pränataldiagnostik

Seltene Tumordispositionssyndrome

Genetic alterations in mature B- and T-cell lymphomas – a practical guide to WHO-HAEM5

Impact of a faulty germinal center reaction on the pathogenesis of primary diffuse large B cell lymphoma of the central nervous system

Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B cell lymphomas

SWI/SNF-Komplex-assoziierte Tumordispositions-Syndrome

Primary adenocarcinoma of the thymus: an immunohistochemical and molecular study with review of the literature

Current molecular and clinical landscape of ATRT: the link to future therapies

No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control

Related objects

Reset password