Hasil Pencarian - Mohammed A Albalwi

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  1. 1
    Genetic Profile of Epidermolysis Bullosa Cases in King Abdulaziz Medical City, Riyadh, Saudi Arabia

    Genetic Profile of Epidermolysis Bullosa Cases in King Abdulaziz Medical City, Riyadh, Saudi Arabia oleh Raghad Alharthi, Raghad Alharthi, Muhannad A. Alnahdi, Muhannad A. Alnahdi, Ahad Alharthi, Seba Almutairi, Seba Almutairi, Sultan Al-Khenaizan, Sultan Al-Khenaizan, Mohammed A. AlBalwi, Mohammed A. AlBalwi, Mohammed A. AlBalwi

    Diterbitkan 2022-02-01
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  2. 2
    Upper limb muscle overgrowth with hypoplasia of the index finger: a new over-growth syndrome caused by the somatic PIK3CA mutation c.3140A>G

    Upper limb muscle overgrowth with hypoplasia of the index finger: a new over-growth syndrome caused by the somatic PIK3CA mutation c.3140A>G oleh Mohammad M. Al-Qattan, Ali Hadadi, Abdullah M. Al-Thunayan, Ahmed A. Eldali, Mohammed A. AlBalwi

    Diterbitkan 2018-09-01
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  3. 3
    Atypical influenza A(H1N1)pdm09 strains caused an influenza virus outbreak in Saudi Arabia during the 2009–2011 pandemic season

    Atypical influenza A(H1N1)pdm09 strains caused an influenza virus outbreak in Saudi Arabia during the 2009–2011 pandemic season oleh Anis Khan, Mohammed A. AlBalwi, Ibraheem AlAbdulkareem, Abdulrahman AlMasoud, Abdulrahman AlAsiri, Wardah AlHarbi, Faisal AlSehile, Aiman El-Saed, Hanan H. Balkhy

    Diterbitkan 2019-07-01
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  4. 4
    Pro106Leu MPL mutation is associated with thrombocytosis and a low risk of thrombosis, splenomegaly and marrow fibrosis

    Pro106Leu MPL mutation is associated with thrombocytosis and a low risk of thrombosis, splenomegaly and marrow fibrosis oleh Musa Alzahrani, Saeed Al Turki, Waleed Al Rajban, Fatimah Alshalati, Fahad Almodaihsh, Khadega A. Abuelgasim, Bader Alahmari, Thamer Al Bogami, Osama Ali, Talal Al Harbi, Mohammed A. AlBalwi, Maram Alotaibi, Aamer Aleem, Ahmed Al Asker, Areej Al Mugairi

    Diterbitkan 2022-11-01
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  5. 5
    Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations.

    Axial Spondylometaphyseal Dysplasia Is Caused by C21orf2 Mutations. oleh Zheng Wang, Aritoshi Iida, Noriko Miyake, Koji M Nishiguchi, Kosuke Fujita, Toru Nakazawa, Abdulrahman Alswaid, Mohammed A Albalwi, Ok-Hwa Kim, Tae-Joon Cho, Gye-Yeon Lim, Bertrand Isidor, Albert David, Cecilie F Rustad, Else Merckoll, Jostein Westvik, Eva-Lena Stattin, Giedre Grigelioniene, Ikuyo Kou, Masahiro Nakajima, Hirohumi Ohashi, Sarah Smithson, Naomichi Matsumoto, Gen Nishimura, Shiro Ikegawa

    Diterbitkan 2016-01-01
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