The Iranian Human Mutation Gene Bank: A data and sample resource for worldwide collaborative genetics research-Reference-Cited by-同舟云学术

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The Iranian Human Mutation Gene Bank: A data and sample resource for worldwide collaborative genetics research

Published:2003-01-27 Issue:2 Volume:21 Page:146-150
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Najmabadi Hossein,Neishabury Maryam,Sahebjam Farhad,Kahrizi Kimia,Shafaghati Yousef,Nikzat Nushin,Jalalvand Maryam,Aminy Farahnaz,Hashemi Susan Bany,Moghimi Babak,Noorian Ali Reza,Jannati Ali,Mohammadi Mehrdad,Javan Khalil

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Linkage of DFNB1 to Non-Syndromic Neurosensory Autosomal-Recessive Deafness in Mediterranean Families

2. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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1. Genetic Crossroads;2021-01-08

2. Narrating ethnicity and diversity in Middle Eastern national genome projects;Social Studies of Science;2018-10

3. Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations;Journal of Genetics;2016-09

4. Huntington’s Disease in Arab Countries;Journal of Huntington's Disease;2015-09-29

5. Molecular Characterization of QDPR Gene in Iranian Families with BH4 Deficiency: Reporting Novel and Recurrent Mutations;JIMD Reports;2015

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