Hasil Pencarian - Javad Mohammadi‐Asl
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AHI1 gene mutation in a consanguineous Iranian family affected by Joubert syndrome: A case report oleh Mostafa Neissi, Hadideh Mabudi, Javad Mohammadi‐Asl
Diterbitkan 2021-10-01
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The worldwide molecular spectrum and distribution of thalassaemia: a systematic review oleh Mina Ebrahimi, Javad Mohammadi-Asl, Fakher Rahim
Diterbitkan 2021-05-01
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A Novel Deleterious MYO15A Gene Mutation Causes Nonsyndromic Hearing Loss oleh Mostafa Neissi, Adnan Al-Badran, Javad Mohammadi-Asl
Diterbitkan 2024-01-01
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An intelligent prenatal screening system for the prediction of Trisomy-21 oleh Amir Jamshidnezhad, Seyed Mohsen Hosseini, Javad Mohammadi-Asl, Mandana Mahmudi
Diterbitkan 2021-01-01
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Evaluation of the effect of oral taurine supplementation on fasting levels of fibroblast growth factors, β-Klotho co-receptor, some biochemical indices and body composition in obes... oleh Fatemeh Haidari, Maryam Asadi, Javad mohammadi-asl, Kambiz Ahmadi-Angali
Diterbitkan 2019-05-01
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Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family oleh Farah Talebi, Farideh Ghanbari Mardasi, Javad Mohammadi Asl, Ali Lashgari, Freidoon Farhadi
Diterbitkan 2018-04-01
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Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family oleh Kourosh Riahi, Farideh Ghanbari Mardasi, Farah Talebi, Farzad Jasemi, Javad Mohammadi Asl
Diterbitkan 2021-10-01
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