檢索結果 - Mohammed S. Al‐Dosari
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Analysis of antioxidative and antiviral biomarkers β-amyrin, β-sitosterol, lupeol, ursolic acid in Guiera senegalensis leaves extract by validated HPTLC methods 由 Mohammad Khalid Parvez, Perwez Alam, Ahmed H. Arbab, Mohammed S. Al‐Dosari, Tawfeq A. Al‐Howiriny, Saleh I. Alqasoumi
出版 2018Artigo -
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POC1A Truncation Mutation Causes a Ciliopathy in Humans Characterized by Primordial Dwarfism 由 Ranad Shaheen, Eissa Faqeih, Hanan E. Shamseldin, Ramil R. Noche, Asma Sunker, Muneera J. Alshammari, Tarfa Al‐Sheddi, Nouran Adly, Mohammed S. Al-Dosari, Sean G. Megason, Muneera Al-Husain, Futwan Al‐Mohanna, Fowzan S. Alkuraya
出版 2012Artigo -
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Prevalence and correlates of autism spectrum disorder in Qatar: a national study 由 Fouad Alshaban, Mohammed S. Al‐Dosari, Hawraa Al‐Shammari, Saba F. Elhag, Iman Ghazal, Mohamed Tolefat, Mogahed Ali, Madeeha Kamal, Nazim Abdel Aati, Mahmoud Abeidah, Ahmad Hassan Saad, Lobna Dekair, Mohanad Al Khasawneh, Katrina Ramsay, Éric Fombonne
出版 2019Artigo -
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Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly 由 Fowzan S. Alkuraya, Xuyu Cai, Carina Emery, Ganeshwaran H. Mochida, Mohammed S. Al‐Dosari, Jillian M. Felie, R. Sean Hill, Brenda J. Barry, Jennifer N. Partlow, Generoso G. Gascon, Amal Y. Kentab, Mohammed M. Jan, Ranad Shaheen, Yuanyi Feng, Christopher A. Walsh
出版 2011Artigo -
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Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families 由 Bashayer Al‐Mubarak, Mohamed Abouelhoda, Aisha Omar, Hesham Aldhalaan, Mohammed S. Al‐Dosari, Michael Nester, Hussain Al-Shamrani, Mohamed El-Kalioby, Ewa Goljan, Renad Albar, Shazia Subhani, Asma I. Tahir, Sultana M. Asfahani, Alaa Eskandrani, Ahmed Almusaiab, Amna Magrashi, Jameela Shinwari, Dorota Monies, Nada Al Tassan
出版 2017Artigo -
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Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number 由 Wen Fan Hu, Oz Pomp, Tawfeg Ben‐Omran, Andrew Kodani, Katrin Henke, Ganeshwaran H. Mochida, Timothy W. Yu, Mollie B. Woodworth, Carine Bonnard, Grace Selva Raj, Thong Teck Tan, Hanan Hamamy, Amira Masri, Mohammad Shboul, Muna Al Saffar, Jennifer N. Partlow, Mohammed S. Al‐Dosari, Anas M. Alazami, Mohammed Al‐Owain, Fowzan S. Alkuraya, Jeremy F. Reiter, Matthew P. Harris, Bruno Reversade, Christopher A. Walsh
出版 2014Artigo -
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Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families 由 Anas M. Alazami, Nisha Patel, Hanan E. Shamseldin, Shamsa Anazi, Mohammed S. Al‐Dosari, Fatema Alzahrani, Hadia Hijazi, Muneera J. Alshammari, Mohammed A. Aldahmesh, Mustafa A. Salih, Eissa Faqeih, Amal Alhashem, Fahad A. Bashiri, Mohammed Al‐Owain, Amal Y. Kentab, Sameera Sogaty, Saeed Al Tala, Mohamad‐Hani Temsah, Maha Tulbah, Rasha Aljelaify, Saad AlShahwan, Mohammed Zain Seidahmed, Adnan A. Alhadid, Hesham Aldhalaan, Fatema AlQallaf, Wesam Kurdi, Majid Alfadhel, Zainab Babay, Mohammad Alsogheer, Namik Kaya, Zuhair N. Al‐Hassnan, Ghada M. H. Abdel‐Salam, Nouriya Al‐Sannaa, Fuad Al Mutairi, Heba Y. El Khashab, Saeed Bohlega, Xiaofei Jia, Henry C. Nguyen, Rakad Hammami, Nouran Adly, Jawahir Y. Mohamed, Firdous Abdulwahab, Niema Ibrahim, Ewa A. Naim, Banan Al‐Younes, Brian F. Meyer, Mais Hashem, Ranad Shaheen, Yong Xiong, Mohamed Abouelhoda, Abdulrahman Aldeeri, Dorota Monies, Fowzan S. Alkuraya
出版 2014Artigo
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