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Publications by Mutaz Amin
Frequency of C.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients With Nonsyndromic Hearing Impairment
Genetics Research International
Genetics
Molecular Biology
Genetic Susceptibility to Asthma and Genetic Interactions in the 5q31-Q33 and 16p11 Regions in Sudanese Families
Immunome Research
Related publications
A Common Founder for the 35delG GJB2 Gene Mutation in Connexin 26 Hearing Impairment
Journal of Medical Genetics
Genetics
Screening of Connexin 26 in Nonsyndromic Hearing Loss
International Archives of Otorhinolaryngology
Otorhinolaryngology
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
Prevalence of Cx26 (GJB2) Gene Mutations Causing Recessive Nonsyndromic Hearing Impairment in India
International Journal of Human Genetics
Genetics
Unauffälliges UNHS-Screening Bei Einem Homozygoten Träger Der 35delG-Mutation Im Connexin 26 Kodierenden Gjb2-Gen
Monatsschrift fur Kinderheilkunde
Child Health
Surgery
Pediatrics
Perinatology
A Novel Splice-Site Mutation in the GJB2 Gene Causing Mild Postlingual Hearing Impairment
PLoS ONE
Multidisciplinary
Rapid Detection of the 35delG Mutation in the GJB2 Gene in Childhood Deafness
Journal of Medical Screening
Health Policy
Public Health
Occupational Health
Environmental
Genetic Counseling for Patients With Nonsyndromic Hearing Impairment Directed by Gene Analysis
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Recurrent Mutations in the Deafness Gene GJB2 (Connexin 26) in British Asian Families
Journal of Medical Genetics
Genetics
