Hasil Pencarian - Abdul Rezzak Hamzeh

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  1. 1
    Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa

    Novel PDE6A mutation in an Emirati patient with retinitis pigmentosa oleh Pratibha Nair, Abdul Rezzak Hamzeh, Ethar Mustafa Malik, Darshjit Oberoi, Mahmoud Taleb Al-Ali, Fatma Bastaki

    Diterbitkan 2017-01-01
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  2. 2
    Identification of a novel CTCF mutation responsible for syndromic intellectual disability – a case report

    Identification of a novel CTCF mutation responsible for syndromic intellectual disability – a case report oleh Fatma Bastaki, Pratibha Nair, Madiha Mohamed, Ethar Mustafa Malik, Mustafa Helmi, Mahmoud Taleb Al-Ali, Abdul Rezzak Hamzeh

    Diterbitkan 2017-06-01
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