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Publications by Camelia Al-Khzouz

GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss

Revista Romana de Medicina de Laborator

2017

English

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Absence of GJB2 Gene Mutations, the GJB6 Deletion (GJB6-D13S1830) and Four Common Mitochondrial Mutations in Nonsyndromic Genetic Hearing Loss in a South African Population

International Journal of Pediatric Otorhinolaryngology

English

GJB3 /GJB6 Screening in GJB2 Carriers With Idiopathic Hearing Loss: Is It Necessary?

Journal of Clinical Laboratory Analysis

Medical Laboratory Technology

Clinical Biochemistry

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Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss

Molecular Medicine Reports

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Screening of GJB6 Gene for the 342-Kb Deletion in Patients From Jordan With Non Syndromic Hearing Loss

International Journal of Human Genetics

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Novel Recessive PDZD7 Biallelic Mutations in Two Chinese Families With Non-Syndromic Hearing Loss

American Journal of Medical Genetics, Part A

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Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss

International Journal of Human Genetics

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Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss

International Journal of Human Genetics

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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

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Novel Mutations Confirm That COL11A2 Is Responsible for Autosomal Recessive Non-Syndromic Hearing Loss DFNB53

Molecular Genetics and Genomics

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Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Camelia Al-Khzouz

GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss

Related publications

Absence of GJB2 Gene Mutations, the GJB6 Deletion (GJB6-D13S1830) and Four Common Mitochondrial Mutations in Nonsyndromic Genetic Hearing Loss in a South African Population

GJB3 /GJB6 Screening in GJB2 Carriers With Idiopathic Hearing Loss: Is It Necessary?

Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss

Screening of GJB6 Gene for the 342-Kb Deletion in Patients From Jordan With Non Syndromic Hearing Loss

Novel Recessive PDZD7 Biallelic Mutations in Two Chinese Families With Non-Syndromic Hearing Loss

Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss

Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss

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

Novel Mutations Confirm That COL11A2 Is Responsible for Autosomal Recessive Non-Syndromic Hearing Loss DFNB53