Items where Author is "Alasti, Fatemeh."

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Article

Vanwesemael, Maarten. and Schrauwen, Isabelle. and Ceuppens, Ruben. and Alasti, Fatemeh. and Jorssen, Ellen. and Farrokhi, Effat. and Hashemzadeh-Chaleshtori, Morteza. and Van Camp, Guy. (2011) A 1 bp 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, 155A (8). pp. 2021-2023.

Vanwesemael, Maarten. and Schrauwen, Isabelle and Ceuppens, Ruben. and Alasti, Fatemeh. and Jorssen, Ellen. and Farrokhi, Effat. and Hashemzadeh-Chaleshtori, Morteza. and Van Camp, Guy. (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, Mohammad Amin. and Alasti, Fatemeh. and Shariati, Laleh. and Farrokhi, Effat. and Fransen, Erik. and Nooridaloii, MohammadReza. and Hashemzadeh-Chaleshtori, Morteza. and Camp, Guy.Van. (2011) DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment. CLINICAL GENETICS, 79 (6). pp. 594-598.

Tabatabaiefar, Mohammad Amin. and Montazer Zohouri, Mostafa. and Alasti, Fatemeh. and Shariati, Laleh. and Farrokhi, Effat. and Farhud, D.D. and Camp, Guy.Van. and Noori-Daloii, M.R. and Hashemzadeh-Chaleshtori, Morteza. (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).

Tabatabaiefar, Mohammad Amin. and Alasti, Fatemeh. and Montazer Zohouri, Mostafa. and Shariati, Laleh. and Farrokhi, Effat. and Farhud, D.D. and Camp, Guy.Van. and Noori-Daloii, Mohammad Reza. and Hashemzadeh-Chaleshtori, Morteza. (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, Abdolrahim. and Sanati, Mohammad Hossein. and Alasti, Fatemeh. and Hashemzadeh-Chaleshtori, Morteza. and Mahmoudian, Saeid. and Ataei, Mitra. (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.

Sadeghi, Abdolrahim. and Sanati, Mohammad Hossein. and Alasti, Fatemeh. and Ataei, Mitra. and Hashemzadeh-Chaleshtori, Morteza. (2005) Mutation analysis of connexin 26 gene and del (GJB6-D13S1830) in patients with hereditary deafness from two provinces in Iran. IRANIAN JOURNAL OF BIOTECHNOLOGY, 3 (4).

This list was generated on Wed May 23 01:08:56 2018 IRDT.