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Publications by Mariem Bensaid
Novel Mutations Confirm That COL11A2 Is Responsible for Autosomal Recessive Non-Syndromic Hearing Loss DFNB53
Molecular Genetics and Genomics
Medicine
Genetics
Molecular Biology
Related publications
Mutation of COL11A2 Causes Autosomal Recessive Non-Syndromic Hearing Loss at the DFNB53 Locus
Journal of Medical Genetics
Genetics
Novel Recessive PDZD7 Biallelic Mutations in Two Chinese Families With Non-Syndromic Hearing Loss
American Journal of Medical Genetics, Part A
Genetics
Genotype-Phenotype Correlation Analysis of MYO15A Variants in Autosomal Recessive Non-Syndromic Hearing Loss
BMC Medical Genetics
Genetics
Identification of a Novel Homozygous Mutation, TMPRSS3: C.535G>A, in a Tibetan Family With Autosomal Recessive Non-Syndromic Hearing Loss
PLoS ONE
Multidisciplinary
Two Novel Mutations Confirm FGD1 Is Responsible for the Aarskog Syndrome
European Journal of Human Genetics
Genetics
DFNB20: A Novel Locus for Autosomal Recessive, Non-Syndromal Sensorineural Hearing Loss Maps to Chromosome 11q25–qter
European Journal of Human Genetics
Genetics
Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of C.299-300delAT Mutation in Kurdish Population of Iran
Journal of audiology and otology
Otorhinolaryngology
Sensory Systems
Speech
Hearing
Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss
Zahedan Journal of Research in Medical Sciences
GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss
Revista Romana de Medicina de Laborator
