H. Ibrahim

EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss

C. Petit, J. Hardelin, M. Dahmani, 2015, Orphanet Journal of Rare Diseases.

Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing

C. Petit, D. Weil, J. Hardelin, 2015, Molecular genetics & genomic medicine.

Frequency of the 35delG allele causing nonsyndromic recessive deafness in the Algerian patients.

F. Ammar-Khodja, M. Makrelouf, A. Zenati, 2007, Genetic counseling.