Majid Fardaei and Medical Genetics - Free people check

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A case report: Autosomal recessive microcephaly caused by a novel...

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Majid Fardaei b, Milad Gholami a, Mohammad Miryounesi ca Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran;

A Case Report with a Mutation in TRIOBP Gene - PubMed

pubmed.ncbi.nlm.nih.gov

by M Fardaei · · Cited by 9 — Authors. Majid Fardaei , Shaghayegh Sarrafzadeh , Soudeh Ghafouri-Fard , Mohammad Miryounesi. Affiliations. 1 Department of Medical Genetics, ... by SK Alashti · — Authors. Shayan Khalili Alashti , Jafar Fallahi , Arezoo Jokar , Majid Fardaei. Affiliations. 1 Department of Medical Genetics, Shiraz University of Medical ... › ...

VSX1 and SOD1 Mutation Screening in Patients with Keratoconus in the...

www.ncbi.nlm.nih.gov

... for funding this research. We also thank the patients for participating in this study. The study was conducted in the Comprehensive Medical Genetics Centre, Shiraz, Iran. The present article was extracted from a thesis written by Payam Naghash. This thesis was supervised by Dr. Mahmood Nejabat and Dr. Majid Fardaei.

An immunocompetent patient with a nonsense mutation in ...bmcmedgenet.biomedcentral.com › articles

bmcmedgenet.biomedcentral.com

Comprehensive Medical Genetic Center, Shiraz University of Medical Sciences, Shiraz, Iran. Majid Fardaei. Department of Medical Genetics, ...

All web results to the name "Majid Fardaei"

Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a...

ijmcmed.org

Autosomal Recessive Nonsyndromic Hearing Loss: A Case Report with a Mutation in TRIOBP Gene · Majid Fardaei 1, Shaghayegh Sarrafzadeh 2, Soudeh Ghafouri-Fard *3, Mohammad Miryounesi Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran., Department of Medical Genetics, ...

A new ATP7B gene mutation with severe condition in two unrelated...

www.infona.pl

Majid Fardaei. Department of Medical Genetics and Molecular Medicine, Shiraz University of Medical Sciences, Shiraz, Iran , .ir. Bibliografia.

[PDF] DNA Sequence Fragment Containing C to A Mutation as a...

www.semanticscholar.org

Hassan Dastsooz 1, Nazanin Vahedi 1, Majid Fardaei 1*. 1Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran. A R T I C L E I N F O. A B S T R A C T. Article type: Short communication. Objective(s): Denaturing high performance liquid chromatography (DHPLC) is a high throughput.

A New Mutation in WT1 Gene Associated with Wilms Tumor ...

brieflands.com

Majid Fardaei , avatar Seyed Mohammad Bagher Tabei , avatar Soudeh Ghafouri-Fard ORCID , avatar Mohammad Miryounesi. 1 Department of Medical Genetics, ... › ijcm › articles

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