Marzieh Mohseni and Kimia Kahrizi - Free people check

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جستجوی نویسنده «Sanaz Arzhangi - Magiranwww.magiran.com › author

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Goli Kazemi, Fatemeh Peymani, Marzieh Mohseni, Farzane Zare Ashrafi, Sanaz Arzhangi, Fariba Ardalani, Fatemeh Aghakhani Moghaddam, Kimia Kahrizi, ...

CiteSeerX — c © Indian Academy of Sciences RESEARCH NOTE...

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@MISC{Naghavi_c©, author = {Anoosh Naghavi and Carla Nishimura and Kimia Kahrizi and Yasser Riazalhosseini and Marzieh Mohseni and Richard J. H. Smith and …

EBSCOhost | | Identification of SLC26A4 gene mutations in...

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Kimia Kahrizi & Marzieh Mohseni & Carla Nishimura &. Niloofar Bazazzadegan & Stephanie M. Fischer &. Atefeh Dehghani & Morteza Sayfati & Maryam ...

Identification of a founder mutation for Pendred syndrome in families ...pubmed.ncbi.nlm.nih.gov › ...

pubmed.ncbi.nlm.nih.gov

Authors. Marzieh Mohseni , Asal Honarpour , Reza Mozafari , Behzad Davarnia , Hossein Najmabadi , Kimia Kahrizi. Affiliations. 1 Genetics Research Center, ...

Identification of SLC26A4 gene mutations in Iranian families with...

www.ncbi.nlm.nih.gov

Kimia Kahrizi,1Marzieh Mohseni,1 Carla Nishimura,2 Niloofar Bazazzadegan,1 Stephanie M. Fischer,2 Atefeh Dehghani,3 Morteza Sayfati,3 Maryam Taghdiri,3 Payman Jamali,3 Richard J. H. Smith,2 Fereydoun Azizi,4 and Hossein Najmabadi1. 1Genetics Research Center, University of Social Welfare ...

Sensorineural deafness and male infertility: a contiguous gene...

core.ac.uk

By Yuzhou Zhang, Mahdi Malekpour, Navid Al-Madani, Kimia Kahrizi, Marvam Zanganeh, Marzieh Mohseni, Faezeh Mojahedi, Ahmad Daneshi, Hossein ...

Autosomal recessive mental retardation: homozygosity mapping...

link.springer.com

Andreas Walter Kuss • Masoud Garshasbi • Kimia Kahrizi • Andreas Tzschach • Farkhondeh Behjati •. Hossein Darvish • Lia Abbasi-Moheb • Lucia Puettmann • Agnes Zecha • Robert Weißmann • Hao Hu •. Marzieh Mohseni • Seyedeh Sedigheh Abedini • Anna Rajab • Christoph Hertzberg • Dagmar ...