Search Results - Ramezanzadeh, Mahboubeh

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  1. 1
    Novel compound heterozygous variants in XYLT1 gene caused Desbuquois dysplasia type 2 in an aborted fetus: a case report

    Novel compound heterozygous variants in XYLT1 gene caused Desbuquois dysplasia type 2 in an aborted fetus: a case report by Rajabi, Fatemeh, Bereshneh, Ali Hosseini, Ramezanzadeh, Mahboubeh, Garshasbi, Masoud

    Published in BMC pediatrics
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  2. 2
    Psychometric of physicians' awareness, attitudes and performance questionnaire about genetic counseling and testing

    Psychometric of physicians' awareness, attitudes and performance questionnaire about genetic counseling and testing by Mousavinasab, SeyyedeMaryam, Khosravi, Sharifeh, Ramezanzadeh, Mahboubeh

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  3. 3
    The Impact of Functional Promoter Variants in Interleukin-18 on Susceptibility to Rheumatoid Arthritis in Iranian Population

    The Impact of Functional Promoter Variants in Interleukin-18 on Susceptibility to Rheumatoid Arthritis in Iranian Population by Ramezanzadeh, Mahboubeh, Khodabandehloo, Fatemeh, Alesaeidi, Samira, Mousavi, Seyyed Hossein, Sadeghi, Shahryar, Ehtesham, Naeim, Mosallaei, Meysam, Hazrati, Ebrahim

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  4. 4
    Cell-free Fetal Nucleic Acid Identifier Markers in Maternal Circulation

    Cell-free Fetal Nucleic Acid Identifier Markers in Maternal Circulation by Ramezanzadeh, Mahboubeh, Khosravi, Sharifeh, Salehi, Rasoul

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  5. 5
    Assessment of high resolution melt analysis feasibility for evaluation of beta-globin gene mutations as a reproducible, cost-efficient and fast alternative to the present conventional method

    Assessment of high resolution melt analysis feasibility for evaluation of beta-globin gene mutations as a reproducible, cost-efficient and fast alternative to the present conventio... by Ramezanzadeh, Mahboubeh, Salehi, Mansour, Salehi, Rasoul

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  6. 6
    Detection of paternally inherited fetal point mutations for β-thalassemia in maternal plasma using simple fetal DNA enrichment protocol with or without whole genome amplification: an accuracy assessment

    Detection of paternally inherited fetal point mutations for β-thalassemia in maternal plasma using simple fetal DNA enrichment protocol with or without whole genome amplification:... by Ramezanzadeh, Mahboubeh, Salehi, Mansour, Farajzadegan, Ziba, Kamali, Sara, Salehi, Rasoul

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