Items where Author is "Ardalani, F."

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Mohseni, M. and Babanejad, M. and Booth, K.T. and Jamali, P. and Jalalvand, K. and Davarnia, B. and Ardalani, F. and Khoshaeen, A. and Arzhangi, S. and Ghodratpour, F. and Beheshtian, M. and Jahanshad, F. and Otukesh, H. and Bahrami, F. and Seifati, S.M. and Bazazzadegan, N. and Habibi, F. and Behravan, H. and Mirzaei, S. and Keshavarzi, F. and Nikzat, N. and Mehrjoo, Z. and Thiele, H. and Nothnagel, M. and Azaiez, H. and Smith, R.J. and Kahrizi, K. and Najmabadi, H. (2021) Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran. Clinical Genetics, 100 (1). pp. 59-78.

Sloan-Heggen, C.M. and Babanejad, M. and Beheshtian, M. and Simpson, A.C. and Booth, K.T. and Ardalani, F. and Frees, K.L. and Mohseni, M. and Mozafari, R. and Mehrjoo, Z. and Jamali, L. and Vaziri, S. and Akhtarkhavari, T. and Bazazzadegan, N. and Nikzat, N. and Arzhangi, S. and Sabbagh, F. and Otukesh, H. and Seifati, S.M. and Khodaei, H. and Taghdiri, M. and Meyer, N.C. and Daneshi, A. and Farhadi, M. and Kahrizi, K. and Smith, R.J.H. and Azaiez, H. and Najmabadi, H. (2015) Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. Journal of Medical Genetics, 52 (12). pp. 823-829.

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