Hasil Pencarian - Maha Alshalan

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  1. 1
    Attitudes to prenatal diagnosis and termination of pregnancy for fetal abnormalities in Saudi couples: a single center experience

    Attitudes to prenatal diagnosis and termination of pregnancy for fetal abnormalities in Saudi couples: a single center experience oleh Maha Alshalan, Majid Alfadhel

    Diterbitkan 2019-12-01
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  2. 2
    Case Report: Clinical delineation of CACNA1D mutation: New cases and literature review

    Case Report: Clinical delineation of CACNA1D mutation: New cases and literature review oleh Alshaimaa Alzahrani, Maha Alshalan, Mohammed Alfurayh, Abdulaziz Bin Akrish, Najlaa A. Alsubeeh, Fuad Al Mutairi, Fuad Al Mutairi

    Diterbitkan 2023-04-01
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  3. 3
    Novel mutation of the FHL1 gene associated with congenital myopathy and early respiratory muscles involvement: a case report

    Novel mutation of the FHL1 gene associated with congenital myopathy and early respiratory muscles involvement: a case report oleh Rana Almutairi, Sara Alrashidi, Muhammed Umair, Maha Alshalan, Lamia Alsubaie, Taghrid Aloraini, Ahmed Al Ahmad, Ahmed Alfares, Fuad Al Mutairi

    Diterbitkan 2020-06-01
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  4. 4
    Biallelic HMGXB4 loss-of-function variant causes intellectual disability, developmental delay, and dysmorphic features

    Biallelic HMGXB4 loss-of-function variant causes intellectual disability, developmental delay, and dysmorphic features oleh Fuad Al Mutairi, Faisal Joueidi, Maha Alshalan, Essra Aloyouni, Mariam Ballow, Mohammed Aldrees, Abdulkareem Al Abdulrahman, Abeer Al Tuwaijri, Safdar Abbas, Muhammad Umair, Majid Alfadhel

    Diterbitkan 2024-08-01
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