Showing 1 - 5 results of 5 for search 'Ibrahim Baydoun', query time: 0.03s Refine Results
  1. 1
    Spectrum of genetic variants in bilateral sensorineural hearing loss

    Spectrum of genetic variants in bilateral sensorineural hearing loss by Amanat Ali, Mohammed Tabouni, Praseetha Kizhakkedath, Ibrahim Baydoun, Mushal Allam, Anne John, Faiza Busafared, Ayesha Alnuaimi, Fatma Al-Jasmi, Fatma Al-Jasmi, Hiba Alblooshi

    Published 2024-02-01
    Get full text
    Article
  2. 2
    Case report: Birk–Landau–Perez syndrome linked to the SLC30A9 gene—identification of additional cases and expansion of the phenotypic spectrum

    Case report: Birk–Landau–Perez syndrome linked to the SLC30A9 gene—identification of additional cases and expansion of the phenotypic spectrum by Praseetha Kizhakkedath, Watfa AlDhaheri, Ibrahim Baydoun, Mohammed Tabouni, Anne John, Taleb M. Almansoori, Saeed Al-Turki, Fatma Al-Jasmi, Fatma Al-Jasmi, Hiba Alblooshi

    Published 2023-07-01
    Get full text
    Article
  3. 3
    Novel compound heterozygous variants (c.971delA/c.542C > T) in SLC1A4 causes spastic tetraplegia, thin corpus callosum, and progressive microcephaly: a case report and mutational analysis

    Novel compound heterozygous variants (c.971delA/c.542C > T) in SLC1A4 causes spastic tetraplegia, thin corpus callosum, and progressive microcephaly: a case report and mutational a... by Feda E. Mohamed, Mohammad A. Ghattas, Mohammad A. Ghattas, Taleb M. Almansoori, Mohammed Tabouni, Ibrahim Baydoun, Praseetha Kizhakkedath, Anne John, Hiba Alblooshi, Qudsia Shaukat, Fatma Al-Jasmi, Fatma Al-Jasmi

    Published 2023-07-01
    Get full text
    Article
  4. 4
    Identification and functional characterisation of a novel DNASE1L3 variant (c.572A>G, p.Asn191Ser) in three Emirati families with systemic lupus erythematosus and hypocomplementaemic urticarial vasculitis

    Identification and functional characterisation of a novel DNASE1L3 variant (c.572A>G, p.Asn191Ser) in three Emirati families with systemic lupus erythematosus and hypocomplementaem... by Najla Aljaberi, Anjali Bharathan, Remya Prajesh Gopal, Ekhlass Mohammed, Fatema Al Shibli, Mohammed Tabouni, Sara Alhmoudi, Praseetha Kizhakkedath, Ibrahim Baydoun, Mushal Allam, Noor Mustafa, Fatma Aljasmi, Afra Al Dhaheri, Hiba Alblooshi

    Published 2025-01-01
    Get full text
    Article
  5. 5
    Profiling genetic variants in cardiovascular disease genes among a Heterogeneous cohort of Mendelian conditions patients and electronic health records

    Profiling genetic variants in cardiovascular disease genes among a Heterogeneous cohort of Mendelian conditions patients and electronic health records by Nadia Akawi, Nadia Akawi, Ghadeera Al Mansoori, Anwar Al Zaabi, Andrea Badics, Noura Al Dhaheri, Noura Al Dhaheri, Aisha Al Shamsi, Amal Al Tenaiji, Amal Al Tenaiji, Bashar Alzohily, Fatmah S. A. Almesmari, Hamad Al Hammadi, Nahid Al Dhahouri, Manal Irshaid, Praseetha Kizhakkedath, Fatema Al Shibli, Mohammed Tabouni, Mushal Allam, Mushal Allam, Ibrahim Baydoun, Hiba Alblooshi, Bassam R. Ali, Roger S. Foo, Roger S. Foo, Fatma Al Jasmi

    Published 2024-10-01
    Get full text
    Article

Search Tools: