Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Hossein Naddafnia
Frequency of GJB 2 Mutations, GJB 6‐D13S1830 and GJB 6‐D13S1854 Deletions Among Patients With Non‐syndromic Hearing Loss From the Central Region of Iran
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Related publications
Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
Genetics
Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
Genetics
GJB2 ‐related Hearing Loss in Central Iran: Review of the Spectrum and Frequency of Gene Mutations
Annals of Human Genetics
Genetics
Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss
Revista Romana de Medicina de Laborator
Novel Recessive PDZD7 Biallelic Mutations in Two Chinese Families With Non-Syndromic Hearing Loss
American Journal of Medical Genetics, Part A
Genetics
Screening of GJB6 Gene for the 342-Kb Deletion in Patients From Jordan With Non Syndromic Hearing Loss
International Journal of Human Genetics
Genetics
GJB 遺伝子変異による難聴児の聴力の検討
AUDIOLOGY JAPAN
Frequency of Mitochondrial Mutations in Non-Syndromic Hearing Loss as Well as Possibly Responsible Variants Found by Whole Mitochondrial Genome Screening
Journal of Human Genetics
Genetics
