Works matching AU Khan, O. A.


Results: 234
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    Molecular characterization of Joubert syndrome in Saudi Arabia.

    Published in:
    Human Mutation, 2012, v. 33, n. 10, p. 1423, doi. 10.1002/humu.22134
    By:
    • Alazami, Anas M.;
    • Alshammari, Muneera J.;
    • Salih, Mustafa A.;
    • Alzahrani, Fatema;
    • Hijazi, Hadia;
    • Seidahmed, Mohammed Z.;
    • Abu Safieh, Leen;
    • Aldosary, Mazhor;
    • Khan, Arif O.;
    • Alkuraya, Fowzan S.
    Publication type:
    Article
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    IMAGING FROM THE INSIGHT LANDER.

    Published in:
    LPI Contribution, 2019, p. 1
    By:
    • Maki, J.;
    • Trebi-Ollennu, A.;
    • Banerdt, B.;
    • Sorice, C.;
    • Bailey, P.;
    • Khan, O.;
    • Kim, W.;
    • Ali, K.;
    • Lim, G.;
    • Deen, R.;
    • Abarca, H.;
    • Ruoff, N.;
    • Hollins, G.;
    • Andres, P.;
    • Hall, J.
    Publication type:
    Article
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    Response To Greenstein’s letter.

    Published in:
    European Journal of Neurology, 2001, v. 8, n. 5, p. 505, doi. 10.1046/j.1468-1331.2001.00259.x
    By:
    • Khan, O. A.;
    • Tselis, A. C.;
    • Kamholz, J. A.;
    • Garbern, J. Y.;
    • Lewis, R. A.;
    • Lisak, R. P.
    Publication type:
    Article
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    Anaesthesia and saccadic eye movements.

    Published in:
    Anaesthesia, 2000, v. 55, n. 9, p. 877, doi. 10.1046/j.1365-2044.2000.01529.x
    By:
    • Khan, O. A.;
    • Taylor, S. R. J.;
    • Jones, J. G.
    Publication type:
    Article
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    Phaeochromocytomas of the bladder.

    Published in:
    Journal of the Royal Society of Medicine, 1982, v. 75, n. 1, p. 17, doi. 10.1177/014107688207500105
    By:
    • Khan, O.;
    • Williams, Gordon;
    • Chisholm, G. D.;
    • Welbourn, R. B.
    Publication type:
    Article
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    Electrostatic correlations fold DNA.

    Published in:
    Biopolymers, 1999, v. 49, n. 2, p. 121, doi. 10.1002/(SICI)1097-0282(199902)49:2<121::AID-BIP1>3.0.CO;2-2
    By:
    • Khan, Malek O.;
    • Jönsson, Bo
    Publication type:
    Article
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    Increasing the Yield in Targeted Next-Generation Sequencing by Implicating CNV Analysis, Non-Coding Exons and the Overall Variant Load: The Example of Retinal Dystrophies.

    Published in:
    PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0078496
    By:
    • Eisenberger, Tobias;
    • Neuhaus, Christine;
    • Khan, Arif O.;
    • Decker, Christian;
    • Preising, Markus N.;
    • Friedburg, Christoph;
    • Bieg, Anika;
    • Gliem, Martin;
    • Issa, Peter Charbel;
    • Holz, Frank G.;
    • Baig, Shahid M.;
    • Hellenbroich, Yorck;
    • Galvez, Alberto;
    • Platzer, Konrad;
    • Wollnik, Bernd;
    • Laddach, Nadja;
    • Ghaffari, Saeed Reza;
    • Rafati, Maryam;
    • Botzenhart, Elke;
    • Tinschert, Sigrid
    Publication type:
    Article
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    New Findings in a Global Approach to Dissect the Whole Phenotype of <i>PLA2G6</i> Gene Mutations.

    Published in:
    PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0076831
    By:
    • Salih, Mustafa A.;
    • Mundwiller, Emeline;
    • Khan, Arif O.;
    • AlDrees, Abdulmajeed;
    • Elmalik, Salah A.;
    • Hassan, Hamdy H.;
    • Al-Owain, Mohammed;
    • Alkhalidi, Hisham M. S.;
    • Katona, Istvan;
    • Kabiraj, Mohammad M.;
    • Chrast, Roman;
    • Kentab, Amal Y.;
    • Alzaidan, Hamad;
    • Rodenburg, Richard J.;
    • Bosley, Thomas M.;
    • Weis, Joachim;
    • Koenig, Michel;
    • Stevanin, Giovanni;
    • Azzedine, Hamid
    Publication type:
    Article
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    Biallelic occult macular dystrophy.

    Published in:
    Ophthalmic Genetics, 2024, v. 45, n. 4, p. 401, doi. 10.1080/13816810.2024.2352376
    By:
    • Ghali, Noor;
    • Khan, Arif O
    Publication type:
    Article
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