Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
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In: 10.1186/s13148-021-01020-w
- Event
-
Veröffentlichung
- (where)
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Aachen
- (who)
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Universitätsbibliothek der RWTH Aachen
- (when)
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2021
- Creator
- DOI
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10.18154/RWTH-CONV-247048
- URN
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urn:nbn:de:101:1-2022072303263535322650
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:36 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Eggermann, Thomas
- Begemann, Matthias
- Pfeiffer, Lutz
- Universitätsbibliothek der RWTH Aachen
Time of origin
- 2021
Other Objects (12)
Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains
Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure
Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation
Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation
First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions
Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders : Characterization of Basic Mechanisms to Improve Clinical Management
Prenatal testing for Imprinting Disorders : A clinical perspective
Molecular mechanisms of human overgrowth and use of omics in its diagnostics : chances and challenges
Growth restriction and genomic imprinting-overlapping phenotypes support the concept of an imprinting network
Corrigendum to: Clinical spectrum and management of imprinting disorders
Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients
Prenatal testing for imprinting disorders : A laboratory perspective
Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains
Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure
Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation
Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation
First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions
Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders : Characterization of Basic Mechanisms to Improve Clinical Management
Prenatal testing for Imprinting Disorders : A clinical perspective
Molecular mechanisms of human overgrowth and use of omics in its diagnostics : chances and challenges
Growth restriction and genomic imprinting-overlapping phenotypes support the concept of an imprinting network
Corrigendum to: Clinical spectrum and management of imprinting disorders
Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients
Prenatal testing for imprinting disorders : A laboratory perspective
Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains
Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure
Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation
Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation
First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions
Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders : Characterization of Basic Mechanisms to Improve Clinical Management
Prenatal testing for Imprinting Disorders : A clinical perspective
Molecular mechanisms of human overgrowth and use of omics in its diagnostics : chances and challenges
Growth restriction and genomic imprinting-overlapping phenotypes support the concept of an imprinting network
Corrigendum to: Clinical spectrum and management of imprinting disorders
Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients