Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: 10.1186/s13148-022-01259-x
- Ereignis
-
Veröffentlichung
- (wo)
-
Aachen
- (wer)
-
Universitätsbibliothek der RWTH Aachen
- (wann)
-
2022
- Urheber
-
Eggermann, Thomas
Yapici, Elzem
Bliek, Jet
Pereda, Arrate
Begemann, Matthias
Russo, Silvia
Tannorella, Pierpaola
Calzari, Luciano
de Nanclares, Guiomar Perez
Lombardi, Paola
Temple, I. Karen
Mackay, Deborah
Riccio, Andrea
Kagami, Masayo
Ogata, Tsutomu
Lapunzina, Pablo
Monk, David
Maher, Eamonn R.
Tümer, Zeynep
- DOI
-
10.18154/RWTH-CONV-249332
- URN
-
urn:nbn:de:101:1-2022112300375940106553
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:24 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Eggermann, Thomas
- Yapici, Elzem
- Bliek, Jet
- Pereda, Arrate
- Begemann, Matthias
- Russo, Silvia
- Tannorella, Pierpaola
- Calzari, Luciano
- de Nanclares, Guiomar Perez
- Lombardi, Paola
- Temple, I. Karen
- Mackay, Deborah
- Riccio, Andrea
- Kagami, Masayo
- Ogata, Tsutomu
- Lapunzina, Pablo
- Monk, David
- Maher, Eamonn R.
- Tümer, Zeynep
- Universitätsbibliothek der RWTH Aachen
Entstanden
- 2022
Ähnliche Objekte (12)
Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions
Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains
Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders : Characterization of Basic Mechanisms to Improve Clinical Management
Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains
Prenatal testing for Imprinting Disorders : A clinical perspective
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
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis
Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions
Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains
Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders : Characterization of Basic Mechanisms to Improve Clinical Management
Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains
Prenatal testing for Imprinting Disorders : A clinical perspective
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
Multi-locus imprinting disturbance (MLID): interim joint statement for clinical and molecular diagnosis
Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure
Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach
First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions
Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains
Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders : Characterization of Basic Mechanisms to Improve Clinical Management
Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains
Prenatal testing for Imprinting Disorders : A clinical perspective
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