Items where Author is "Abdollahnejad, F."
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Number of items: 2.
(2018) Frequency of gjb2 mutations in families with autosomal recessive non-syndromic hearing loss in Khuzestan province. Genetika. pp. 837-846. ISSN 05340012 (ISSN)
(2017) A novel TECTA mutation causes ARNSHL. International Journal of Pediatric Otorhinolaryngology. pp. 88-93. ISSN 0165-5876