Search Results - Najafabadi, Shima Zamanian

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  1. 1
    Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population

    Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population by Abolhassani, Ayda, Fattahi, Zohreh, Beheshtian, Maryam, Fadaee, Mahsa, Vazehan, Raheleh, Ahangari, Fatemeh, Dehdahsi, Shima, Faraji Zonooz, Mehrshid, Parsimehr, Elham, Kalhor, Zahra, Peymani, Fatemeh, Mozaffarpour Nouri, Maryam, Babanejad, Mojgan, Noudehi, Khadijeh, Fatehi, Fatemeh, Zamanian Najafabadi, Shima, Afroozan, Fariba, Yazdan, Hilda, Bozorgmehr, Bita, Azarkeivan, Azita, Sadat Mahdavi, Shokouh, Nikuei, Pooneh, Fatehi, Farzad, Jamali, Payman, Ashrafi, Mahmoud Reza, Karimzadeh, Parvaneh, Habibi, Haleh, Kahrizi, Kimia, Nafissi, Shahriar, Kariminejad, Ariana, Najmabadi, Hossein

    Published in Npj genomic medicine
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  2. 2
    Comprehensive copy number analysis of spinal muscular atrophy among the Iranian population

    Comprehensive copy number analysis of spinal muscular atrophy among the Iranian population by Khanbazi, Ali, Beheshtian, Maryam, Azad, Maryam, Akbari Kelishomi, Masoumeh, Afroozan, Fariba, Fatehi, Fatemeh, Noudehi, Khadijeh, Zamanian Najafabadi, Shima, Omrani, Mohammadamin, Habibi, Haleh, Taghdiri, Maryam, Abdi Rad, Isa, Nafissi, Shahriar, Jankhah, Aria, Yazdan, Hilda, Daneshmand, Parvaneh, Saberi, Seyed Hosseinali, Kahrizi, Kimia, Kariminejad, Ariana, Najmabadi, Hossein

    Published in Scientific reports
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  3. 3
    P483: A comprehensive study of spinal muscular atrophy testing referrals’ data among the Iranian population since 2006

    P483: A comprehensive study of spinal muscular atrophy testing referrals’ data among the Iranian population since 2006 by Khanbazi, Ali, Beheshtian, Maryam, Azad, Maryam, Akbari, Masoume, Afrozan, Fariba, Fatehi, Fatemeh, Noudehi, Khadijeh, Najafabadi, Shima Zamanian, Kariminejad, Ariana, Kahrizi, Kimia, Najmabadi, Hossein

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  4. 4
    P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders

    P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders by Abolhassani, Ayda, Fattahi, Zohreh, Beheshtian, Maryam, Fadaee, Mahsa, Vazehan, Raheleh, Ahangari, Fatemeh, Dehdahsi, Shima, Zonooz, Mehrshid Faraji, Parsimehr, Elham, Kalhor, Zahra, Peymani, Fatemeh, Nouri, Maryam Mozaffarpour, Babanejad, Mojgan, Noudehi, Khadijeh, Fatehi, Fatemeh, Najafabadi, Shima Zamanian, Afroozan, Fariba, Yazdan, Hilda, Bozorgmehr, Bita, Azarkeivan, Azita, Mahdavi, Shokouh Sadat, Nikuei, Pooneh, Fatehi, Farzad, Jamali, Payman, Ashrafi, Mahmoud Reza, Karimzadeh, Parvaneh, Habibi, Haleh, Kahrizi, Kimia, Nafissi, Shahriar, Kariminejad, Ariana, Najmabadi, Hossein

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