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LinkedIn: Majid Fardaei - Iran - LinkedIn
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BigData/x028 at master · Kulikovpavel/BigData · GitHub
github.com
web intel and big data hw3, bat files - latest, mincemeat.py work much faster that octo.py - Kulikovpavel/BigData
Loop | Majid Fardaei
loop.frontiersin.org
A Novel Mutation in ERCC8 Gene Causing …ayne Syndrome. Maryam Taghdiri; Hassan Dastsooz; Majid Fardaei; Sanaz Mohammadi; Mohammad Ali Farazi Fard; Mohammad Ali Faghihi · Frontiers in Pediatrics. Published on 09 Aug views; XXdownloads; XXcitations; View impact · View All Publications ...
bigData-coursera/x028 at master · dhruvgairola/bigData-coursera ·...
github.com
Web Intelligence and Big Data, Gautam Shroff, IIT Delhi - dhruvgairola/bigData-coursera
Coursera/x028 at master · mbecker73/Coursera · GitHub
github.com
This repo is where I am going to dump various programming assignments I have done during courses on Coursera - Coursera/x028 at master · mbecker73/Coursera
big_data/x028 at master · sevenmaxis/big_data · GitHub
github.com
Homework for Big Data Coursera course. Contribute to sevenmaxis/big_data development by creating an account on GitHub.
A case report: Autosomal recessive microcephaly caused by a novel...
www.sciencedirect.com
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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