Items where Author is "Reiisi, S."

Article

(2019) Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations. Iranian Journal of Public Health. pp. 1704-1713. ISSN 2251-6085

(2018) GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants. International Journal of Pediatric Otorhinolaryngology. pp. 121-126. ISSN 0165-5876

(2018) Investigation of the association between (CCTTT)n polymorphism in NOS2 gene and serum IgE level in patients with vernal keratoconjunctivitis in Chaharmahal va Bakhtiari Province. Gene Reports. pp. 165-170. ISSN 2452-0144

(2017) Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran. Iranian Journal of Public Health. pp. 76-82. ISSN 2251-6085

(2017) A novel TECTA mutation causes ARNSHL. International Journal of Pediatric Otorhinolaryngology. pp. 88-93. ISSN 0165-5876

(2016) Genetic linkage analysis of DFNB40 and DFNB48 loci in families with autosomal recessive non-syndromic hearing loss (ARNSHL) from western provinces of Iran. Journal of Isfahan Medical School. ISSN 10277595 (ISSN)

(2016) Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family. Iranian Journal of Basic Medical Sciences. pp. 772-778. ISSN 2008-3866

(2015) Genetic linkage analysis of the DFNB63 locus in families with autosomal recessive nonsyndromic hearing loss from Hamadan and Kohgiluyeh and Boyer-Ahmad Provinces, Iran. Journal of Isfahan Medical School. pp. 1308-1317. ISSN 10277595 (ISSN)

(2015) Mutation screening of 3’UTR and exons 1-2 of vsx1 gene by PCR-SSCP/HA and sequencing in patients with Vernal Keratoconjuctivis (VKC) in Shahrekord. Journal of Zanjan University of Medical Sciences and Health Services. ISSN 16069366 (ISSN)

(2015) Screening BRCA1 and BRCA2 Mutation Frequencies In Breast Cancer Patients Of West Iran Reveals a Novel Polymorphism In BRCA1 Gene. European Journal of Oncology. pp. 94-99. ISSN 11286598 (ISSN)