Work

Xp21 deletion in female patients with intellectual disability: Two new cases and a review of the literature

Year: 2015

Type: article

Study design: Case Report

Source: European Journal of Medical Genetics

DOI: 10.1016/j.ejmg.2015.04.003

Authors: Solveig Heide, Alexandra Afenjar, Patrick Edery, Damien Sanlaville, Boris Keren, Alexandre Rouen, Alinoë Lavillaureix, Capucine Hyon, Diane Doummar, Jean-Pierre Siffroi, Sandra Chantot-Bastaraud

Institutions: Hôpital Armand-Trousseau, Assistance Publique – Hôpitaux de Paris, Lyon 1 Université, Inserm, Centre de Recherche en Neurosciences de Lyon, Hospices Civils de Lyon, Pitié-Salpêtrière Hospital

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W1970347358

FWCI: 7.444

Cites: 28

Cited by: 58

Related to: 10