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Christine Petit
Christine Petit
University of Paris
Medicine
Audiology
Exome sequencing
Consanguinity
Genetics
3
Papers
23
Citations
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PHENOTYPIC CHARACTERISTICS OF ROD–CONE DYSTROPHY ASSOCIATED WITH MYO7A MUTATIONS IN A LARGE FRENCH COHORT
2019
Retina-the Journal of Retinal and Vitreous Diseases
Samer Khateb
Saddek Mohand-Said
Marco Nassisi
Crystel Bonnet
Anne Françoise Roux
Camille Andrieu
Aline Antonio
Christel Condroyer
Christina Zeitz
Céline Devisme
Natalie Loundon
Sandrine Marlin
Christine Petit
Bahram Bodaghi
José-Alain Sahel
Isabelle Audo
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Citations (8)
Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa province
2018
International Journal of Pediatric Otorhinolaryngology
Sonia Talbi
Crystel Bonnet
Zied Riahi
Farid Boudjenah
Malika Dahmani
Jean-Pierre Hardelin
Fabienne Wong Jun Tai
Malek Louha
Fatima Ammar-Khodja
Christine Petit
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Citations (6)
A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family
2016
International Journal of Pediatric Otorhinolaryngology
Asma Behlouli
Crystel Bonnet
Samia Abdi
Mokhtar Hasbellaoui
Farid Boudjenah
Jean-Pierre Hardelin
Malek Louha
Mohamed Makrelouf
Fatima Ammar-Khodja
Akila Zenati
Christine Petit
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Citations (9)
1