Items where Author is "Nadeali, Z."

Article

(2024) Molecular and phenotypical findings of a novel de novo SYNGAP1 gene variant in an 11-year-old Iranian boy with intellectual disability. Laboratory medicine. pp. 204-208. ISSN 1943-7730 (Electronic) 0007-5027 (Linking)

(2024) A novel de novo frameshift variant in the CHD2 gene related to intellectual and developmental disability, seizures and speech problems. Molecular Genetics & Genomic Medicine. e2305. ISSN 2324-9269 (Electronic) 2324-9269 (Linking)

(2022) Possible role of pannexin 1 channels and purinergic receptors in the pathogenesis and mechanism of action of SARS-CoV-2 and therapeutic potential of targeting them in COVID-19. LIFE SCIENCES. ISSN 0024-3205 1879-0631 J9 - LIFE SCI

(2018) Estimating the Risk for Chromosomal Abnormalities and Heteromorphic Variants in Azoospermic and Severe Oligozoospermic Men. Crescent Journal of Medical and Biological Sciences. pp. 101-106. ISSN 2148-9696

(2015) Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran. International Journal of Pediatric Otorhinolaryngology. pp. 1892-1895. ISSN 0165-5876

(2015) Significant association between nonsyndromic cleft lip with or without cleft palate and IRF6rs2235371 polymorphism in Iranian familiar population. Molecular Biology. pp. 848-851. ISSN 0026-8933