Hasil Pencarian - zahra tabatabaei
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Analysis of Market Reaction to Risk Disclosure Factors oleh zahra tabatabaei, Seyed Abbas Hashemi, Hadi Amiri
Diterbitkan 2022-09-01
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Toward More Transparent and Accurate Cancer Diagnosis With an Unsupervised CAE Approach oleh Zahra Tabatabaei, Adrian Colomer, Javier Oliver Moll, Valery Naranjo
Diterbitkan 2023-01-01
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WWFedCBMIR: World-Wide Federated Content-Based Medical Image Retrieval oleh Zahra Tabatabaei, Yuandou Wang, Adrián Colomer, Javier Oliver Moll, Zhiming Zhao, Valery Naranjo
Diterbitkan 2023-09-01
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Advancing Content-Based Histopathological Image Retrieval Pre-Processing: A Comparative Analysis of the Effects of Color Normalization Techniques oleh Zahra Tabatabaei, Fernando Pérez Bueno, Adrián Colomer, Javier Oliver Moll, Rafael Molina, Valery Naranjo
Diterbitkan 2024-03-01
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Pre-Implantation Genetic Testing for Monogenic Disorders (PGT-M) in A Family with A Novel Mutation in DPAGT1 Gene oleh Zahra Tabatabaei, Khadijeh Karbalaie, Parham Habibzadeh, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi, Mohammad-Hossein Nasr Esfahani
Diterbitkan 2021-10-01
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Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay oleh Parham Habibzadeh, Zahra Tabatabaei, Soroor Inaloo, Muhammad Mahdi Nashatizadeh, Matthis Synofzik, Matthis Synofzik, Vahid Reza Ostovan, Mohammad Ali Faghihi, Mohammad Ali Faghihi
Diterbitkan 2020-12-01
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A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: a case report oleh Hossein Esmaeilzadeh, Mohammad Reza Bordbar, Hassan Dastsooz, Mohammad Silawi, Mohammad Ali Farazi Fard, Ali Adib, Ali Kafashan, Zahra Tabatabaei, Forough Sadeghipour, Mohammad Ali Faghihi
Diterbitkan 2018-07-01
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Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT gene oleh Parham Habibzadeh, Zahra Tabatabaei, Mohammad Ali Farazi Fard, Laila Jamali, Aazam Hafizi, Pooneh Nikuei, Leila Salarian, Mohammad Hossein Nasr Esfahani, Zahra Anvar, Mohammad Ali Faghihi
Diterbitkan 2020-02-01
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Prenatal diagnosis of Sex determining region Y -box transcription factor 2 anophthalmia syndrome caused by germline mosaicism using next-generation sequencing: A case report oleh Pooneh Nikuei, Ph.D., Zahra Khashavy, Mohammad Ali Farazi Fard, Shahrzad Tabasi4 Pharm.D. Student, Ari Zeidi5 B.Sc. Student, Parnian Pourkashani, Zahra Tabatabaei, Ebrahim Eftekhar, Mozhgan Saberi, Frouzandeh Mahjoubi
Diterbitkan 2023-09-01
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