Search Results - Elsayed, Liena Elbaghir Omer

  • Showing 1 - 4 results of 4
Refine Results
  1. 1
    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
    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  2. 2
    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
    Get full text
    Article
    Save to List
    Saved in:
  3. 3
    A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease

    A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease by Elsayed, Liena Elbaghir Omer, Drouet, Valérie, Usenko, Tatiana, Mohammed, Inaam N., Hamed, Ahlam AbdAlrahman Ahmed, Elseed, Maha Abdelmoneim, Salih, Mustafa A.M., Koko, Mahmoud Eltayeb, Mohamed, Ashraf Yahia Osman, Siddig, Rayan Abubaker, Elbashir, Mustafa Idris, Ibrahim, Muntaser Eltayeb, Durr, Alexandra, Stevanin, Giovanni, Lesage, Suzanne, Ahmed, Ammar Eltahir, Brice, Alexis

    Published in Annals of neurology
    Get full text
    Article
    Save to List
    Saved in:
  4. 4
    A N ovel N onsense M utation in DNAJC 6 E xpands the P henotype of A utosomal‐ R ecessive J uvenile‐ O nset P arkinson's D isease

    A N ovel N onsense M utation in DNAJC 6 E xpands the P henotype of A utosomal‐ R ecessive J uvenile‐ O nset P arkinson's D isease by Elsayed, Liena Elbaghir Omer, Drouet, Valérie, Usenko, Tatiana, Mohammed, Inaam N., Hamed, Ahlam AbdAlrahman Ahmed, Elseed, Maha Abdelmoneim, Salih, Mustafa A.M., Koko, Mahmoud Eltayeb, Mohamed, Ashraf Yahia Osman, Siddig, Rayan Abubaker, Elbashir, Mustafa Idris, Ibrahim, Muntaser Eltayeb, Durr, Alexandra, Stevanin, Giovanni, Lesage, Suzanne, Ahmed, Ammar Eltahir, Brice, Alexis

    Published in Annals of neurology
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:

Search Tools: