CP
Christine Petit

Publications (6)

Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Article scientifique · 2024
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Article scientifique · 2024
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
Article scientifique · 2021
Genetic Heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB Variants Detected Among Hearing Impaired Families in Morocco
Article scientifique · 2021
A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders
Article scientifique · 2017
Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome
Article scientifique · 2016

Domaines principaux

Sciences de la santé5 Sciences de la vie et biotechnologies1

Statistiques

Consultations10
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