Hasil Pencarian - Humaira Ayub

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  1. 1
    Prescribing Patterns of Antibiotics in Tertiary Care Hospital of Abbottabad, Khyber Pakhtunkhwa

    Prescribing Patterns of Antibiotics in Tertiary Care Hospital of Abbottabad, Khyber Pakhtunkhwa oleh Fiaz Alam, Palwasha Zahid, Humaira Ayub, Muhammad Atif, Rabbia Aslam

    Diterbitkan 2024-05-01
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  2. 2
    Prescribing Patterns of Antibiotics in Tertiary Care Hospital of Abbottabad, Khyber Pakhtunkhwa

    Prescribing Patterns of Antibiotics in Tertiary Care Hospital of Abbottabad, Khyber Pakhtunkhwa oleh Fiaz Alam, Palwasha Zahid, Humaira Ayub, Muhammad Atif, Rabbia Aslam

    Diterbitkan 2024-05-01
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  3. 3
    Prescribing Patterns of Antibiotics in Tertiary Care Hospital of Abbottabad, Khyber Pakhtunkhwa

    Prescribing Patterns of Antibiotics in Tertiary Care Hospital of Abbottabad, Khyber Pakhtunkhwa oleh Fiaz Alam, Palwasha Zahid, Humaira Ayub, Muhammad Atif, Rabbia Aslam

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  4. 4
    Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma.

    Variants in the ASB10 Gene Are Associated with Primary Open Angle Glaucoma. oleh Shazia Micheal, Humaira Ayub, Farrah Islam, Sorath Noorani Siddiqui, Wajid Ali Khan, Farah Akhtar, Raheel Qamar, Muhammad Imran Khan, Anneke I den Hollander

    Diterbitkan 2015-01-01
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  5. 5
    Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucoma.

    Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucoma. oleh Humaira Ayub, Shazia Micheal, Farah Akhtar, Muhammad Imran Khan, Shaheena Bashir, Nadia K Waheed, Mahmood Ali, Frederieke E Schoenmaker-Koller, Sobia Shafique, Raheel Qamar, Anneke I den Hollander

    Diterbitkan 2014-01-01
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  6. 6
    Exome sequencing identifies three novel candidate genes implicated in intellectual disability.

    Exome sequencing identifies three novel candidate genes implicated in intellectual disability. oleh Zehra Agha, Zafar Iqbal, Maleeha Azam, Humaira Ayub, Lisenka E L M Vissers, Christian Gilissen, Syeda Hafiza Benish Ali, Moeen Riaz, Joris A Veltman, Rolph Pfundt, Hans van Bokhoven, Raheel Qamar

    Diterbitkan 2014-01-01
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  7. 7
    Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.

    Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families. oleh Sobia Shafique, Saima Siddiqi, Margit Schraders, Jaap Oostrik, Humaira Ayub, Ammad Bilal, Muhammad Ajmal, Celia Zazo Seco, Tim M Strom, Atika Mansoor, Kehkashan Mazhar, Syed Tahir A Shah, Alamdar Hussain, Maleeha Azam, Hannie Kremer, Raheel Qamar

    Diterbitkan 2014-01-01
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  8. 8
    Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.

    Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan. oleh Maleeha Maria, Muhammad Ajmal, Maleeha Azam, Nadia Khalida Waheed, Sorath Noorani Siddiqui, Bilal Mustafa, Humaira Ayub, Liaqat Ali, Shakeel Ahmad, Shazia Micheal, Alamdar Hussain, Syed Tahir Abbas Shah, Syeda Hafiza Benish Ali, Waqas Ahmed, Yar Muhammad Khan, Anneke I den Hollander, Lonneke Haer-Wigman, Rob W J Collin, Muhammad Imran Khan, Raheel Qamar, Frans P M Cremers

    Diterbitkan 2015-01-01
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