Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1868-7083
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci ; volume:8 ; number:1 ; day:7 ; month:3 ; year:2016 ; pages:1-3 ; date:12.2016
Clinical epigenetics ; 8, Heft 1 (7.3.2016), 1-3, 12.2016
- Urheber
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Eggermann, Thomas
- Beteiligte Personen und Organisationen
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de Nanclares, Guiomar Perez
Maher, Eamonn R.
Temple, I. Karen
Tümer, Zeynep
Monk, David
Mackay, Deborah J. G.
Grønskov, Karen
Riccio, Andrea
Linglart, Agnès
Netchine, Irène
SpringerLink (Online service)
- DOI
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10.1186/s13148-016-0194-5
- URN
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urn:nbn:de:1111-2016031023937
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
07.01.20232023, 16:40 MEZ
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Beteiligte
- Eggermann, Thomas
- de Nanclares, Guiomar Perez
- Maher, Eamonn R.
- Temple, I. Karen
- Tümer, Zeynep
- Monk, David
- Mackay, Deborah J. G.
- Grønskov, Karen
- Riccio, Andrea
- Linglart, Agnès
- Netchine, Irène
- SpringerLink (Online service)
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Corrigendum to: Clinical spectrum and management of imprinting disorders
Prenatal testing for imprinting disorders : A laboratory perspective
Growth restriction and genomic imprinting-overlapping phenotypes support the concept of an imprinting network
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
Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains
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Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation
Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci
Prenatal testing for Imprinting Disorders : A clinical perspective
Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure
Molecular and Clinical Opposite Findings in 11p15.5 Associated Imprinting Disorders : Characterization of Basic Mechanisms to Improve Clinical Management
Corrigendum to: Clinical spectrum and management of imprinting disorders
Prenatal testing for imprinting disorders : A laboratory perspective
Growth restriction and genomic imprinting-overlapping phenotypes support the concept of an imprinting network
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
Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains
Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation