Showing 1 - 7 results of 7 for search 'Mohammad A. Alshabeeb', query time: 0.04s Refine Results
  1. 1
    Pharmacogenes that demonstrate high association evidence according to CPIC, DPWG, and PharmGKB

    Pharmacogenes that demonstrate high association evidence according to CPIC, DPWG, and PharmGKB by Mohammad A. Alshabeeb, Mohammad A. Alshabeeb, Mesnad Alyabsi, Mesnad Alyabsi, Mohammad A. Aziz, Salah Abohelaika

    Published 2022-10-01
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  2. 2
    Use of Pharmacogenetic Drugs by the Dutch Population

    Use of Pharmacogenetic Drugs by the Dutch Population by Mohammad A. Alshabeeb, Mohammad A. Alshabeeb, Mohammad A. Alshabeeb, Vera H. M. Deneer, Amjad Khan, Amjad Khan, Folkert W. Asselbergs, Folkert W. Asselbergs, Folkert W. Asselbergs

    Published 2019-07-01
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  3. 3
    Prevalence of exposure to pharmacogenetic drugs by the Saudis treated at the health care centers of the Ministry of National Guard

    Prevalence of exposure to pharmacogenetic drugs by the Saudis treated at the health care centers of the Ministry of National Guard by Mohammad A. Alshabeeb, Mesnad Alyabsi, Bien Paras

    Published 2022-08-01
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  4. 4
    Impact of telemedicine on glycemic control in type 2 diabetes mellitus during the COVID-19 lockdown period

    Impact of telemedicine on glycemic control in type 2 diabetes mellitus during the COVID-19 lockdown period by Abrar M. Al-Mutairi, Abrar M. Al-Mutairi, Abrar M. Al-Mutairi, Mohammad A. Alshabeeb, Mohammad A. Alshabeeb, Mohammad A. Alshabeeb, Salah Abohelaika, Fadhel A. Alomar, Keshore R. Bidasee, Keshore R. Bidasee, Keshore R. Bidasee

    Published 2023-02-01
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  5. 5
    Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

    Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10 by Amjad Khan, Rongrong Wang, Shirui Han, Muhammad Umair, Safdar Abbas, Muhammad Ismail Khan, Mohammad A. Alshabeeb, Majid Alfadhel, Xue Zhang

    Published 2019-10-01
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  6. 6
    Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10

    Correction to: Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10 by Amjad Khan, Rongrong Wang, Shirui Han, Muhammad Umair, Safdar Abbas, Muhammad Ismail Khan, Mohammad A. Alshabeeb, Majid Alfadheland, Xue Zhang

    Published 2019-12-01
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  7. 7
    A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani Family

    A Novel Homozygous Nonsense Mutation p.Cys366* in the WNT10B Gene Underlying Split-Hand/Split Foot Malformation in a Consanguineous Pakistani Family by Amjad Khan, Amjad Khan, Amjad Khan, Rongrong Wang, Shirui Han, Muhammad Umair, Mohammad A. Alshabeeb, Muhammad Ansar, Wasim Ahmad, Manal Alaamery, Xue Zhang, Xue Zhang

    Published 2020-01-01
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