Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing
Ammar‐Khodja, Fatima, Bonnet, Crystel, Dahmani, Malika, Ouhab, Sofiane, Lefèvre, Gaelle M., Ibrahim, Hassina, Hardelin, Jean‐Pierre, Weil, Dominique, Louha, Malek, Petit, Christine
Published in Molecular genetics & genomic medicine (01.05.2015)
Published in Molecular genetics & genomic medicine (01.05.2015)
Get full text
Journal Article
The spectrum of GJB2 gene mutations in Algerian families with nonsyndromic hearing loss from Sahara and Kabylie regions
Talbi, Sonia, Bonnet, Crystel, Boudjenah, Farid, Mansouri, Mohammed Tahar, Petit, Christine, Ammar Khodja, Fatima
Published in International journal of pediatric otorhinolaryngology (01.09.2019)
Published in International journal of pediatric otorhinolaryngology (01.09.2019)
Get full text
Journal Article
A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family
Behlouli, A, Bonnet, C, Abdi, S, Hasbellaoui, M, Boudjenah, F, Hardelin, J.-P, Louha, M, Makrelouf, M, Ammar-Khodja, F, Zenati, A, Petit, C
Published in International journal of pediatric otorhinolaryngology (01.08.2016)
Published in International journal of pediatric otorhinolaryngology (01.08.2016)
Get full text
Journal Article
Molecular screening of deafness in Algeria: High genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F
Ammar-Khodja, Fatima, Faugère, Valérie, Baux, David, Giannesini, Claire, Léonard, Susana, Makrelouf, Mohamed, Malek, Rahia, Djennaoui, Djamel, Zenati, Akila, Claustres, Mireille, Roux, Anne-Françoise
Published in European journal of medical genetics (01.07.2009)
Published in European journal of medical genetics (01.07.2009)
Get full text
Journal Article
ATP6V1B1 recurrent mutations in Algerian deaf patients associated with renal tubular acidosis
Dahmani, Malika, Talbi, Sonia, Ammar-Khodja, Fatima, Ouhab, Sofiane, Boudjenah, Farid, Djebbar, Merieme, Bonnet, Crystel, Petit, Christine
Published in International journal of pediatric otorhinolaryngology (01.02.2020)
Published in International journal of pediatric otorhinolaryngology (01.02.2020)
Get full text
Journal Article
Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa province
Talbi, Sonia, Bonnet, Crystel, Riahi, Zied, Boudjenah, Farid, Dahmani, Malika, Hardelin, Jean-Pierre, Wong Jun Tai, Fabienne, Louha, Malek, Ammar-Khodja, Fatima, Petit, Christine
Published in International journal of pediatric otorhinolaryngology (01.09.2018)
Published in International journal of pediatric otorhinolaryngology (01.09.2018)
Get full text
Journal Article
EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss
Dahmani, Malika, Ammar-Khodja, Fatima, Bonnet, Crystel, Lefèvre, Gaelle M, Hardelin, Jean-Pierre, Ibrahim, Hassina, Mallek, Zahia, Petit, Christine
Published in Orphanet journal of rare diseases (19.08.2015)
Published in Orphanet journal of rare diseases (19.08.2015)
Get full text
Journal Article
The cytogenetic aspect of male infertility
Ammar-Khodja, Fatima, Hamouli, Zohra, Boukerbout, Fella F, Djerroudib, Karima
Published in International journal of reproductive biomedicine (Yazd, Iran) (01.12.2014)
Get full text
Published in International journal of reproductive biomedicine (Yazd, Iran) (01.12.2014)
Journal Article
FREQUENCY OF THE 35delG ALLELE CAUSING NON-SYNDROMIC RECESSIVE DEAFNESS IN THE ALGERIAN PATIENTS
Ammar-Khodja, F, Makrelouf, M, Malek, R, Ibrahim, H, Zenati, A
Published in Genetic counseling (01.01.2007)
Get full text
Published in Genetic counseling (01.01.2007)
Journal Article
The cytogenetic aspect of male infertility
Ammar-Khodja, Fatima, Hamouli, Zohra, Boukerbout F, Fella, Djerroudib, Karima
Published in Iranian journal of reproductive medicine (01.12.2014)
Get full text
Published in Iranian journal of reproductive medicine (01.12.2014)
Journal Article