Hasil Pencarian - Shahid Mahmood Baig

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  1. 1
    Tumor Necrosis Factor Alpha SNP Variant in Promoter Region G308a, cause Preeclampsia during Pregnancy in Pakistani Women, A Case Control Study

    Tumor Necrosis Factor Alpha SNP Variant in Promoter Region G308a, cause Preeclampsia during Pregnancy in Pakistani Women, A Case Control Study oleh Azizah Ziauddin, Sadia Ahmad, Asad Iqbal, Abdul Majid Khan, Shahid Mahmood Baig

    Diterbitkan 2020-12-01
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  2. 2
    Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families

    Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families oleh Yingjie Zhou, Muhammad Tariq, Sijie He, Uzma Abdullah, Jianguo Zhang, Shahid Mahmood Baig

    Diterbitkan 2020-07-01
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  3. 3
    Fine mapping of MRT9 locus through genome wide homozygosity mapping in a consanguineous Pakistani family

    Fine mapping of MRT9 locus through genome wide homozygosity mapping in a consanguineous Pakistani family oleh Shoaib Ur Rehman, Shahid Mahmood Baig, Larse Hasen, Ilyas Ahmad, Rahmat Ali, Masroor Hussain

    Diterbitkan 2019-11-01
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  4. 4
    Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosis.

    Autosomal recessive transmission of a rare KRT74 variant causes hair and nail ectodermal dysplasia: allelism with dominant woolly hair/hypotrichosis. oleh Doroteya Raykova, Joakim Klar, Aysha Azhar, Tahir Naeem Khan, Naveed Altaf Malik, Muhammad Iqbal, Muhammad Tariq, Shahid Mahmood Baig, Niklas Dahl

    Diterbitkan 2014-01-01
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  5. 5
    Whole exome sequencing identified a homozygous novel variant in DOP1A gene in the Pakistan family with neurodevelopmental disabilities: case report and literature review

    Whole exome sequencing identified a homozygous novel variant in DOP1A gene in the Pakistan family with neurodevelopmental disabilities: case report and literature review oleh Wei Zhang, Wei Zhang, Muhammad Tariq, Bhaskar Roy, Juan Shen, Juan Shen, Ayaz Khan, Naveed Altaf Malik, Sijie He, Sijie He, Shahid Mahmood Baig, Xiaodong Fang, Xiaodong Fang, Xiaodong Fang, Jianguo Zhang

    Diterbitkan 2024-05-01
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  6. 6
    Role of cholesterol and sphingolipids in brain development and neurological diseases

    Role of cholesterol and sphingolipids in brain development and neurological diseases oleh Ghulam Hussain, Jing Wang, Azhar Rasul, Haseeb Anwar, Ali Imran, Muhammad Qasim, Shamaila Zafar, Syed Kashif Shahid Kamran, Aroona Razzaq, Nimra Aziz, Waseem Ahmad, Asghar Shabbir, Javed Iqbal, Shahid Mahmood Baig, Tao Sun

    Diterbitkan 2019-01-01
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  7. 7
    The interleukin-11 receptor variant p.W307R results in craniosynostosis in humans

    The interleukin-11 receptor variant p.W307R results in craniosynostosis in humans oleh Ilyas Ahmad, Juliane Lokau, Birte Kespohl, Naveed Altaf Malik, Shahid Mahmood Baig, Roland Hartig, Daniel Behme, Roland Schwab, Janine Altmüller, Muhammad Jameel, Sören Mucha, Holger Thiele, Muhammad Tariq, Peter Nürnberg, Jeanette Erdmann, Christoph Garbers

    Diterbitkan 2023-08-01
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  8. 8
    Sensitive detection of pre-existing BCR-ABL kinase domain mutations in CD34+ cells of newly diagnosed chronic-phase chronic myeloid leukemia patients is associated with imatinib resistance: implications in the post-imatinib era.

    Sensitive detection of pre-existing BCR-ABL kinase domain mutations in CD34+ cells of newly diagnosed chronic-phase chronic myeloid leukemia patients is associated with imatinib re... oleh Zafar Iqbal, Aamer Aleem, Mudassar Iqbal, Mubashar Iqbal Naqvi, Ammara Gill, Abid Sohail Taj, Abdul Qayyum, Najeeb ur-Rehman, Ahmad Mukhtar Khalid, Ijaz Hussain Shah, Muhammad Khalid, Riazul Haq, Mahwish Khan, Shahid Mahmood Baig, Abid Jamil, Muhammad Naeem Abbas, Muhammad Absar, Amer Mahmood, Mahmood Rasool, Tanveer Akhtar

    Diterbitkan 2013-01-01
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  9. 9
    An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan

    An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan oleh Sajida Rasool, Jamshaid Mahmood Baig, Abubakar Moawia, Ilyas Ahmad, Maria Iqbal, Syeda Seema Waseem, Maria Asif, Uzma Abdullah, Ehtisham Ul Haq Makhdoom, Emrah Kaygusuz, Muhammad Zakaria, Shafaq Ramzan, Saif ul Haque, Asif Mir, Iram Anjum, Mehak Fiaz, Zafar Ali, Muhammad Tariq, Neelam Saba, Wajid Hussain, Birgit Budde, Saba Irshad, Angelika Anna Noegel, Stefan Höning, Shahid Mahmood Baig, Peter Nürnberg, Muhammad Sajid Hussain

    Diterbitkan 2020-09-01
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