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Publications by Jair Mantovani
Screening of Connexin 26 in Nonsyndromic Hearing Loss
International Archives of Otorhinolaryngology
Otorhinolaryngology
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Connexin-26–associated Deafness: Phenotypic Variability and Progression of Hearing Loss
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Frequency of C.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients With Nonsyndromic Hearing Impairment
Genetics Research International
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Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss
Molecular Medicine Reports
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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
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Presymptomatic Diagnosis of Nonsyndromic Hearing Loss by Genotyping
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Histopathology of Nonsyndromic Autosomal Dominant Midfrequency Sensorineural Hearing Loss
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Screening of the Connexin 26 (35delg) Mutation in Egyptian Patients With Autosomal Recessive Nonsyndromic Deafness and Its Relation to the Patients' Iq
Egyptian Journal of Genetics and Cytology
Etiologic Diagnosis of Nonsyndromic Genetic Hearing Loss in Adult vs Pediatric Populations
Otolaryngology - Head and Neck Surgery
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