Work

Possible association between complex congenital heart defects and 11p15 hypomethylation in three patients with severe Silver–Russell syndrome

Year: 2013

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics Part A

DOI: 10.1002/ajmg.a.35691

Authors: Mustafa Ghanim, Sylvie Rossignol, Bruno Delobel, Melita Irving, Owen Miller, Louise Devisme, Jean‐Louis Plennevaux, Sophie Lucidarme‐Rossi, Sylvie Manouvrier, Azzi Salah, Olimpia Chivu, Irène Netchine, Catherine Vincent‐Delorme

Institutions: An-Najah National University, Centre Hospitalier Universitaire de Lille, Groupe Hospitalier de l'Institut Catholique de Lille, Inserm, Hôpital Armand-Trousseau, Université Pierre-et-Marie-Curie, Guy's Hospital, Guy's and St Thomas' NHS Foundation Trust, Evelina London Children's Healthcare, Centre Hospitalier d'Arras

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2104404426

FWCI: 1.416

Cites: 31

Cited by: 23

Related to: 10