Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: Molecular genetics & genomic medicine 6(6), Seiten/Artikel-Nr.:1225-1228, 2018

Event: Veröffentlichung

(where): Aachen

(who): Universitätsbibliothek der RWTH Aachen

(when): 2018

Creator: Eggermann, Thomas
Ledig, Susanne
Begemann, Matthias
Elbracht, Miriam
Kurth, Ingo
Wieacker, Peter

DOI: 10.18154/RWTH-CONV-237210

URN: urn:nbn:de:101:1-2019092406195253774442

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:31 AM CEST

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Associated

Eggermann, Thomas
Ledig, Susanne
Begemann, Matthias
Elbracht, Miriam
Kurth, Ingo
Wieacker, Peter
Universitätsbibliothek der RWTH Aachen

Time of origin

2018

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Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

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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

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Prenatal testing for Imprinting Disorders : A clinical perspective

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

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Growth restriction and genomic imprinting-overlapping phenotypes support the concept of an imprinting network

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Prenatal testing for imprinting disorders : A laboratory perspective

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Search for altered imprinting marks in Mayer-Rokitansky-Küster-Hauser patients

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Other Objects (12)

Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

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

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

Prenatal testing for imprinting disorders : A laboratory perspective

Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

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

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

Prenatal testing for imprinting disorders : A laboratory perspective

Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

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

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Growth restriction and genomic imprinting-overlapping phenotypes support the concept of an imprinting network

Corrigendum to: Clinical spectrum and management of imprinting disorders

Prenatal testing for imprinting disorders : A laboratory perspective

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