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Publications by Samia Abdi
A Novel Biallelic Splice Site Mutation of TECTA Causes Moderate to Severe Hearing Impairment in an Algerian Family
International Journal of Pediatric Otorhinolaryngology
Medicine
Otorhinolaryngology
Pediatrics
Perinatology
Child Health
Related publications
A Novel Splice Site Mutation in theRDXgene Causes DFNB24 Hearing Loss in an Iranian Family
American Journal of Medical Genetics, Part A
Genetics
A Novel Splice-Site Mutation in the GJB2 Gene Causing Mild Postlingual Hearing Impairment
PLoS ONE
Multidisciplinary
Opinions of Hearing Parents About the Causes of Hearing Impairment of Their Children With Biallelic GJB2 Mutations
Journal of Community Genetics
Environmental
Public Health
Genetics
Epidemiology
Occupational Health
A Novel Aberrant Splice Site Mutation in the APC Gene
Journal of Medical Genetics
Genetics
A Novel Mutation in the WFS1gene Identified in a Taiwanese Family With Low-Frequency Hearing Impairment
BMC Medical Genetics
Genetics
Intronic PRRT2 Mutation Generates Novel Splice Acceptor Site and Causes Paroxysmal Kinesigenic Dyskinesia With Infantile Convulsions (PKD/IC) in a Three Generation Family
BMC Medical Genetics
Genetics
A Novel De Novo Mutation in CEACAM16 Associated With Postlingual Hearing Impairment
Molecular Syndromology
Genetics
A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
A Splice Mutation in a Syrian Autosomal Recessive Hypercholesterolemia Family Causes a Two-Nucleotide Deletion of mRNA
Circulation Research
Cardiovascular Medicine
Physiology
Cardiology
