Items where Author is "Alasti, F."

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Article

Vanwesemael, M. and Schrauwen, I. and Ceuppens, R. and Alasti, F. and Jorssen, E. and Farrokhi, E. and Chaleshtori, M.H. and Van Camp, G. (2011) A 1bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame. American Journal of Medical Genetics, Part A, 155 (8). pp. 2021-2023.

Tabatabaiefar, M.A. and Alasti, F. and Shariati, L. and Farrokhi, E. and Fransen, E. and Nooridaloii, M.R. and Chaleshtori, M.H. and Van Camp, G. (2011) DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment. CLINICAL GENETICS, 79 (6). pp. 594-598.

Tabatabaiefar, M.A. and Alasti, F. and Montazer Zohour, M. and Shariati, L. and Farrokhi, E. and Farhud, D.D. and Camp, G.V. and Noori-Daloii, M.R. and Hashemzadeh Chaleshtori, M. (2011) Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss. IRANIAN JOURNAL OF PUBLIC HEALTH, 40 (2). pp. 34-48.

Sadeghi, A. and Sanati, M.H. and Alasti, F. and Chaleshtori, M.H. and Mahmoudian, S. and Ataei, M. (2009) Contribution of GJB2 mutations and Four common DFNB loci in autosomal recessive non-syndromic hearing impairment in Markazi and Qom provinces of Iran. Iranian Journal of Biotechnology, 7 (2). 108-111+120.

This list was generated on Sat Sep 23 01:07:48 2017 IRST.