Search Results - ElTayeb, Yousif Hussein

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  1. 1
    Mosaic trisomy 13 and constitutional delay in puberty

    Mosaic trisomy 13 and constitutional delay in puberty by Eltayeb, Sara Yousif Hussein, Bashier, Alaaeldin, Hussain, Azza Abdulaziz Khalifa Bin

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  2. 2
    A case of small bowel obstruction due to phytobezoars

    A case of small bowel obstruction due to phytobezoars by Ali, Wadah Abdelazim Ahmed, Gondal, Zafar Iqbal, Yammahi, Ali Abdulla Ali Khammas, Hushki, Shadi Faour Ahmed, Badri, Faisal, ElTayeb, Yousif Hussein

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  3. 3
    Mosaic trisomy 13 and constitutional delay in puberty

    Mosaic trisomy 13 and constitutional delay in puberty by Eltayeb, Sara Yousif Hussein, Bashier, Alaaeldin, Hussain, Azza Abdulaziz Khalifa Bin

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  4. 4
    A case of small bowel obstruction due to phytobezoars

    A case of small bowel obstruction due to phytobezoars by Ali, Wadah Abdelazim Ahmed, Gondal, Zafar Iqbal, Yammahi, Ali Abdulla Ali Khammas, Hushki, Shadi Faour Ahmed, Badri, Faisal, ElTayeb, Yousif Hussein

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  5. 5
    Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

    Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype by Elsayed, Liena Elbaghir Omer, AlHarbi, Norah Ayed, Alqarni, Ashwaq Mohammed, Eltayeb, Huda Hussein Elwasila, Mostafa, Noura Mostafa Mohamed, Abdulrahim, Maha Mohammed, Zaid, Hadeel Ibrahim Bin, Alanzi, Latifah Mansour, Ababtain, Sarah Abdullah, Aldulaijan, Khawlah, Aloyouni, Sheka Yagub, Othman, Moneeb Abdullah Kassem, Alkheilewi, Mohammad Abdullah, Binduraihem, Adel Mohammed, Alrukban, Hadeel Abdollah, Ahmed, Hiba Yousif, AlRadini, Faten Abdullah, Alahdal, Hadil Mohammad, Mushiba, Aziza Mufareh, Alzaher, Omaima Abdulazeem

    Published in Human genomics
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  6. 6
    Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

    Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype by Elsayed, Liena Elbaghir Omer, AlHarbi, Norah Ayed, Alqarni, Ashwaq Mohammed, Eltayeb, Huda Hussein Elwasila, Mostafa, Noura Mostafa Mohamed, Abdulrahim, Maha Mohammed, Zaid, Hadeel Ibrahim Bin, Alanzi, Latifah Mansour, Ababtain, Sarah Abdullah, Aldulaijan, Khawlah, Aloyouni, Sheka Yagub, Othman, Moneeb Abdullah Kassem, Alkheilewi, Mohammad Abdullah, Binduraihem, Adel Mohammed, Alrukban, Hadeel Abdollah, Ahmed, Hiba Yousif, AlRadini, Faten Abdullah, Alahdal, Hadil Mohammad, Mushiba, Aziza Mufareh, Alzaher, Omaima Abdulazeem

    Published in Human genomics
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  7. 7
    Blood Glucose, HbA1c Level, and its Correlation with VEGF-A (+405G/C) Polymorphism as Biomarker Predicts the Risk of Retinopathy and Nephropathy in Type 2 Diabetic Patients

    Blood Glucose, HbA1c Level, and its Correlation with VEGF-A (+405G/C) Polymorphism as Biomarker Predicts the Risk of Retinopathy and Nephropathy in Type 2 Diabetic Patients by Yousif Hussin Alimam, Hoyam, Abdelateif Hussein, Waleed, Ibrahim, Sabah, Abdelgani, Sara, Alharthi, Nahed, Bashier Eltayeb, Lienda, Abdelgadir Elmahdi, Salih, Abobakr Abdrabo, AbdElkarim

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