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Publications by Ali Anousheh
A Novel Splice Site Mutation in theRDXgene Causes DFNB24 Hearing Loss in an Iranian Family
American Journal of Medical Genetics, Part A
Genetics
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A Novel Biallelic Splice Site Mutation of TECTA Causes Moderate to Severe Hearing Impairment in an Algerian Family
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Child Health
A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family
BioMed Research International
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Molecular Biology
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A Novel Splice-Site Mutation in the GJB2 Gene Causing Mild Postlingual Hearing Impairment
PLoS ONE
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A Novel Mutation in FGFR3 Causes Camptodactyly, Tall Stature, and Hearing Loss (CATSHL) Syndrome
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A Novel Aberrant Splice Site Mutation in the APC Gene
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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
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Pre-Implantation Genetic Diagnosis in an Iranian Family With a Novel Mutation in MUT Gene
BMC Medical Genetics
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Novel Splice Site IDUA Gene Mutation in Tunisian Pedigrees With Hurler Syndrome
Diagnostic Pathology
Forensic Medicine
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A Novel Loss-Of-Function Mutation in HOXB1 Associated With Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family
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