Marzieh Mohseni and Hossein - Free people check

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50 neue genetische Ursachen für geistige Behinderung entdeckt

www.innovations-report.de

Hossein Najmabadi, Hao Hu, Masoud Garshasbi, Tomasz Zemojtel, Seyedeh Sedigheh Abedini, Wei Chen, Masoumeh Hosseini, Farkhondeh Behjati, Stefan Haas, Payman Jamali, Agnes Zecha, Marzieh Mohseni, Lucia Püttmann, Leyla Nouri Vahid, Corinna Jensen, Lia Abbasi Moheb, Melanie Bienek, ...

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

jmg.bmj.com

Marzieh Mohseni 2, Faezeh Mojahedi 4, Ahmad Daneshi 5, Hossein Najmabadi 2, Richard J H Smith 1; 1 Molecular Otolaryngology Research ...

Einwanderung - Bedrohung oder Zukunft?: Mythen und Fakten zur ...books.google.de › books

books.google.de

(8), (2008), S – Darvish, Hossein/Sahar Esmaeeli-Nieh/Gholamreza. B. Monajemi/Marzieh Mohseni/ Saghar Ghasemi-Firouzabadi/Seyedeh ...

SLC52A2 Mutations Cause SCABD2 Phenotype: A Second Report - Google...

books.google.de

Contributors, Mojgan Babanejad, Omid Ali Adeli, Nooshin Nikzat, Maryam Beheshtian, Hakimeh Azarafra, Farnaz Sadeghnia, Marzieh Mohseni, Hossein ...

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

citeseerx.ist.psu.edu

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

Deep sequencing reveals 50 novel genes for recessive cognitive...

www.scienceopen.com

... Masoumeh Hosseini, Farkhondeh Behjati, Stefan Haas, Payman Jamali, Agnes Zecha, Marzieh Mohseni, Lucia Püttmann, Leyla Nouri Vahid ...

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, ...

Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive...

www.ncbi.nlm.nih.gov

Maryam Beheshtian, MD MPH,1 Mojgan Babanejad, MSc,1 Hela Azaiez, PhD,2 Niloofar Bazazzadegan, MSc,1 Diana Kolbe, PhD,2 Christina Sloan-Heggen, BS,2 Sanaz Arzhangi, BS,1 Kevin Booth, BS,2Marzieh Mohseni, MSc,1 Kathy Frees, BS,2 Mohammad Hossein Azizi, MD,3 Ahmad Daneshi, MD,4 ...

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 ...

Deep sequencing reveals 50 novel genes for recessive ...

www.nature.com

· , Marzieh Mohseni, Leyla Nouri Vahid, Lia Abbasi Moheb, Farzaneh Larti, Hossein Darvish, Saghar Ghasemi Firouzabadi, Zohreh Fattahi, Mohammad Javad Soltani Banavandi ...