Search Results - "M Hashemzadeh Chaleshtori
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1
Congratulation to Margaret Chan Familial and Sporadic GJB2-Related Deafness in Iran: Review of Gene Mutations by M Hashemzadeh Chaleshtori, DD Farhud, MA Patton
Published 2007Call Number: Loading…Connect to this object online.
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2
Congratulation to Margaret Chan Familial and Sporadic GJB2-Related Deafness in Iran: Review of Gene Mutations by M Hashemzadeh Chaleshtori, DD Farhud, MA Patton
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3
Dermatoglyphics in Patients with Oligo/ Azospermia by H Pour-Jafari, M Hashemzadeh Chaleshtori DD Farhud
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4
Dermatoglyphics in Patients with Oligo/ Azospermia by H Pour-Jafari, M Hashemzadeh Chaleshtori DD Farhud
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5
Progress of Education, Research and Services in Medical Genetics, in Some Institutions of Iran by DD Farhud, AS Lotfi, M Hashemzadeh Chaleshtori, M Akhondi, H Sadighi
Published 2009Call Number: Loading…Connect to this object online.
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6
Progress of Education, Research and Services in Medical Genetics, in Some Institutions of Iran by DD Farhud, AS Lotfi, M Hashemzadeh Chaleshtori, M Akhondi, H Sadighi
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7
"Deafness -Associated Connexin 26 Gene (GJB2) Mutations in Iranian Population" by M Hashemzadeh Chaleshtori, DD Farhud, R Taylor, V Hadavi, MA Patton, AR Afzal
Published 2002Call Number: Loading…Connect to this object online.
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8
"Deafness -Associated Connexin 26 Gene (GJB2) Mutations in Iranian Population" by M Hashemzadeh Chaleshtori, DD Farhud, R Taylor, V Hadavi, MA Patton, AR Afzal
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9
Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss by MA Tabatabaiefar, F Alasti, M Montazer Zohour, L Shariati, E Farrokhi, DD Farhud, GV Camp, MR Noori-Daloii, M Hashemzadeh Chaleshtori
Published 2011Call Number: Loading…Connect to this object online.
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10
Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss by MA Tabatabaiefar, F Alasti, M Montazer Zohour, L Shariati, E Farrokhi, DD Farhud, GV Camp, MR Noori-Daloii, M Hashemzadeh Chaleshtori
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11
Report of a New Mutation and Frequency of Connexin 26 gene (GJB2) Mutations in Patients from Three Provinces of Iran by A Hosseinipour, M Hashemzadeh Chaleshtori, R Sasanfar, DD Farhud, A Tolooi, M Doulati, L Hoghooghi Rad, M Montazer zohour, M Ghadami
Published 2005Call Number: Loading…Connect to this object online.
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12
Report of a New Mutation and Frequency of Connexin 26 gene (GJB2) Mutations in Patients from Three Provinces of Iran by A Hosseinipour, M Hashemzadeh Chaleshtori, R Sasanfar, DD Farhud, A Tolooi, M Doulati, L Hoghooghi Rad, M Montazer zohour, M Ghadami
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13
"Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations " by R Sasanfar, A Tolouei, A Hoseinipour, DD Farhud, M Dolati, L Hoghooghi Rad, M Montazer Zohour, M Ghadami, H Pour-Jafari, M Hashemzadeh Chaleshtori
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14
"Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations " by R Sasanfar, A Tolouei, A Hoseinipour, DD Farhud, M Dolati, L Hoghooghi Rad, M Montazer Zohour, M Ghadami, H Pour-Jafari, M Hashemzadeh Chaleshtori
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15
Frequencies of Mutations in the Connexin 26 Gene (GJB2) in Two Populations of Iran (Tehran and Tabriz) by M Hashemzadeh Chaleshtori, L Hoghooghi Rad, M Dolati, R Sasanfar, A Hoseinipour, M Montazer Zohour, H Pourjafari, A Tolooi, M Ghadami, DD Farhud, MA Patton
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16
Frequencies of Mutations in the Connexin 26 Gene (GJB2) in Two Populations of Iran (Tehran and Tabriz) by M Hashemzadeh Chaleshtori, L Hoghooghi Rad, M Dolati, R Sasanfar, A Hoseinipour, M Montazer Zohour, H Pourjafari, A Tolooi, M Ghadami, DD Farhud, MA Patton
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17
"Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations" by "M Hashemzadeh Chaleshtori, M Dowlati, DD Farhud, L Hoghooghi Rad, R Sasanfar A Hoseinipour, M Montazer Zohour, A Tolooi, M Ghadami, HR Pourjafari, MA Oshaghi, MA Patton "
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18
"Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations" by "M Hashemzadeh Chaleshtori, M Dowlati, DD Farhud, L Hoghooghi Rad, R Sasanfar A Hoseinipour, M Montazer Zohour, A Tolooi, M Ghadami, HR Pourjafari, MA Oshaghi, MA Patton "
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19
Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases by M Hashemzadeh Chaleshtori, DD Farhud, AH Crosby, E Farrokhi, H Pour Jafari, K Ghatreh Samani, K Safa Chaleshtori, M Kasiri, M Shahrani, GR Mobini, M Mansouri, D Modarresinia, M Jafari
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20
Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases by M Hashemzadeh Chaleshtori, DD Farhud, AH Crosby, E Farrokhi, H Pour Jafari, K Ghatreh Samani, K Safa Chaleshtori, M Kasiri, M Shahrani, GR Mobini, M Mansouri, D Modarresinia, M Jafari
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