Search Results - Abolfazl Heidari

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    Novel Homozygous Nonsense Mutation in the LRP5 Gene in Two Siblings with Osteoporosis-pseudoglioma Syndrome by Abolfazl Heidari, Ali Homaei, Fatemeh Saffari

    Published 2023
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    Identification of a Novel Mutation in an Iranian Family With 17-β Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Series by Abolfazl Heidari, Ali Homaei, Fatemeh Saffari

    Published 2022
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    Diagnostic value of NIPT assay for fetal aneuploidy screening in pregnant women with moderate risk of trisomy in first stage screening by Fatemeh Lalooha, Shokouh Sadat Haji Seyed Abotorabi, Farideh Movahed, Farzaneh Bahrami, Abolfazl Heidari, Monirsadat Mirzadeh

    Published 2022
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