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Afsaneh Sahebalzamani
Afsaneh Sahebalzamani
Genetics
Genetic heterogeneity
Biology
Dominance (genetics)
CDH23
5
Papers
16
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A Novel VPS13B Mutation Identified by Whole-Exome Sequencing in Iranian Patients with Cohen Syndrome.
2021
Journal of Molecular Neuroscience
Mohammad Reza Karimzadeh
Fatemeh Omidi
Afsaneh Sahebalzamani
Kolsoum Saeidi
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Screening Consanguineous Families for Hearing Loss Using the MiamiOtoGenes Panel.
2020
Genetic Testing and Molecular Biomarkers
Abhiraami Kannan-Sundhari
Denise Yan
Kolsoum Saeidi
Afsaneh Sahebalzamani
Susan H. Blanton
Xue Zhong Liu
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Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis
2018
BioMed Research International
Haiqiong Shang
Denise Yan
Naeimeh Tayebi
Kolsoum Saeidi
Afsaneh Sahebalzamani
Yong Feng
Susan H. Blanton
Xuezhong Liu
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Citations (12)
A Common Ancestral Asn242Ser Mutation in TMEM67 Identified in Multiple Iranian Families with Joubert Syndrome
2017
Public Health Genomics
Mohammadreza Dehghani
Majid Mojarad
Ehsan Ghayoor Karimiani
Mohammad Yahya Vahidi Mehrjardi
Afsaneh Sahebalzamani
Farah Ashrafzadeh
Mehran Beiraghi Toosi
Atiyeh Eslahi
Najmeh Ahangari
Seyed Mojtaba Yassini
Afsaneh Hassanbeigi
Azam Rasti
Seyed Mehdi Kalantar
Reza Maroofian
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Citations (2)
Acrocallosal Syndrome in a 6-Year-Old Iranian Boy
2016
Genetics in the Third Millennium
Afsaneh Sahebalzamani
Ariana Kariminejad
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