Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1868-7083

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: 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

Creator: Eggermann, Thomas

Contributor: 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: 10.1186/s13148-016-0194-5

URN: urn:nbn:de:1111-2016031023937

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:27 AM CEST

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Associated

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)

Other Objects (12)

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

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

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

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Erratum to: Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci

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Other Objects (12)

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

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

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

Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation

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