Search Results - Al Awadi, Maha

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  1. 1
    PB2521: STUDY OF HEMOGLOBIN S-OMAN TRAIT: NEW INSIGHTS

    PB2521: STUDY OF HEMOGLOBIN S-OMAN TRAIT: NEW INSIGHTS by Al-Mahrouqi, Nouh, Al Awadi, Maha, Al Hosni, Aisha, Al Khabori, Murtadha, Al Rawas, Abdul Hakim, Al Rawahi, Mohammed, Al-Rahbi, Ameera, Daar, Shahina, Wali, Yasser

    Published in HemaSphere
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  2. 2
    A biallelic variant of the RNA exosome gene, EXOSC4, associated with neurodevelopmental defects impairs RNA exosome function and translation

    A biallelic variant of the RNA exosome gene, EXOSC4, associated with neurodevelopmental defects impairs RNA exosome function and translation by Fasken, Milo B., Leung, Sara W., Cureton, Lauryn A., Al-Awadi, Maha, Al-Kindy, Adila, van Hoof, Ambro, Khoshnevis, Sohail, Ghalei, Homa, Al-Maawali, Almundher, Corbett, Anita H.

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  3. 3
    The super sickling haemoglobin HbS‐Oman: a study of red cell sickling, K+ permeability and associations with disease severity in patients heterozygous for HbA and HbS‐Oman (HbA/S‐Oman genotype)

    The super sickling haemoglobin HbS‐Oman: a study of red cell sickling, K+ permeability and associations with disease severity in patients heterozygous for HbA and HbS‐Oman (HbA/S‐O... by Al Balushi, Halima W. M., Wali, Yasser, Al Awadi, Maha, Al‐Subhi, Taimoora, Rees, David C., Brewin, John N., Hannemann, Anke, Gibson, John S.

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  4. 4
    A novel mutation in DDR2 causing spondylo-meta-epiphyseal dysplasia with short limbs and abnormal calcifications (SMED-SL) results in defective intra-cellular trafficking

    A novel mutation in DDR2 causing spondylo-meta-epiphyseal dysplasia with short limbs and abnormal calcifications (SMED-SL) results in defective intra-cellular trafficking by Al-Kindi, Adila, Kizhakkedath, Praseetha, Xu, Huifang, John, Anne, Sayegh, Abeer Al, Ganesh, Anuradha, Al-Awadi, Maha, Al-Anbouri, Lamya, Al-Gazali, Lihadh, Leitinger, Birgit, Ali, Bassam R

    Published in BMC genetics
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  5. 5
    Transglutaminase-1 Mutations in Omani Families with Lamellar Ichthyosis

    Transglutaminase-1 Mutations in Omani Families with Lamellar Ichthyosis by Al-Naamani, Aisha, Al-Waily, Ahmed, Al-Kindi, Mohammed, Al-Awadi, Maha, Al-Yahyaee, Said Ali

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  6. 6
    PB2521: STUDY OF HEMOGLOBIN S‐OMAN TRAIT: NEW INSIGHTS

    PB2521: STUDY OF HEMOGLOBIN S‐OMAN TRAIT: NEW INSIGHTS by Al‐Mahrouqi, Nouh, Al Awadi, Maha, Al Hosni, Aisha, Al Khabori, Murtadha, Al Rawas, Abdul Hakim, Al Rawahi, Mohammed, Al‐Rahbi, Ameera, Daar, Shahina, Wali, Yasser

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  7. 7
    Incidence, Clinical Characteristics, and Histopathological Results of Atypia of Undermined Significance in a Tertiary Center in UAE

    Incidence, Clinical Characteristics, and Histopathological Results of Atypia of Undermined Significance in a Tertiary Center in UAE by Shangab, Maha Osman, Khalifa, Azza Abdulaziz, Al Awadi, Fatheya, Alsharhan, Mouza, Bashier, Alaaeldin

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  8. 8
    Trisomy 9 syndrome in a neonate with unusual features

    Trisomy 9 syndrome in a neonate with unusual features by Abu Henedi, Maha M., Muhammad, Fawziyah M., Masud, Hatim A., Abu al-Hasan, Sawsan J., al-Awadi, Sadika A.

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