Items where Author is "Amani Geshnigani, S."

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Hashemzadeh Chaleshtori, M. and Simpson, M.A. and Farrokhi, E. and Dolati, M. and Hoghooghi Rad, L. and Amani Geshnigani, S. and Crosby, A.H. (2007) Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families. CLINICAL GENETICS, 72 (3). pp. 261-263.

This list was generated on Sat Jul 2 01:48:11 2022 IRDT.