F. Ammar-Khodja

ATP6V1B1 recurrent mutations in Algerian deaf patients associated with renal tubular acidosis.

C. Petit, M. Dahmani, Sonia Talbi, 2019, International journal of pediatric otorhinolaryngology.

Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa province.

C. Petit, J. Hardelin, M. Louha, 2018, International journal of pediatric otorhinolaryngology.

A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family.

C. Petit, J. Hardelin, M. Louha, 2016, International journal of pediatric otorhinolaryngology.

Exclusion of chromosomal abnormalities and microdeletions 22q11 and 10p13 in algerian patients with isolated conotruncal malformation

F. Ammar-Khodja, M. Abdellali, 2015, Cytology and Genetics.

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.

Molecular screening of deafness in Algeria: high genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F.

M. Claustres, A. Roux, C. Giannesini, 2009, European journal of medical genetics.

A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family.

C. Petit, J. Hardelin, M. Louha, 2016, International journal of pediatric otorhinolaryngology.