Work

Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader–Willi like features and hypotonia

Year: 2012

Type: article

Study design: Case Report

Source: European Journal of Medical Genetics

DOI: 10.1016/j.ejmg.2012.04.011

Authors: Inesse Ben-Abdallah-Bouhjar, Hanene Hannachi, Audrey Labalme, Abir Gmidène, Soumaya Mougou, Najla Soyah, Moez Gribaa, Damien Sanlaville, Hatem Elghezal, Ali Saad

Institutions: Hôpital Farhat Hached, University of Sousse, Hospices Civils de Lyon

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: W2000267269

FWCI: 0.288

Cites: 34

Cited by: 41

Related to: 10