Hasil Pencarian - Amitha Ananth

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  1. 1
    Compound heterozygous variants within two conserved sialyltransferase motifs of ST3GAL5 cause GM3 synthase deficiency

    Compound heterozygous variants within two conserved sialyltransferase motifs of ST3GAL5 cause GM3 synthase deficiency oleh Natasha Rudy, Kazuhiro Aoki, Amitha Ananth, Lynda Holloway, Cindy Skinner, Anna Hurst, Michael Tiemeyer, Richard Steet

    Diterbitkan 2023-03-01
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  2. 2
    P567: Innovations in education: Empowering child neurology residents with basic concepts in genomic testing through a national curriculum

    P567: Innovations in education: Empowering child neurology residents with basic concepts in genomic testing through a national curriculum oleh Kuntal Sen, Amitha Ananth, Rachel Gottlieb-Smith, Daniel Calalme, Jeffrey Strelzik, Kristin Baranano, Lisa Emrick, Julie Ziobro, Christa Habela, Margie Ream, Divakar Mithal, Andrea Gropman, Louis Dang

    Diterbitkan 2024-01-01
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  3. 3
    Distribution of hand function by age in individuals with Rett syndrome

    Distribution of hand function by age in individuals with Rett syndrome oleh Jeffrey L. Neul, Tim A. Benke, Eric D. Marsh, Jane B. Lane, David N. Lieberman, Steven A. Skinner, Daniel G. Glaze, Bernhard Suter, Peter T. Heydemann, Arthur A. Beisang, Shannon M. Standridge, Robin C. C. Ryther, Richard H. Haas, Lloyd J. Edwards, Amitha Ananth, Alan K. Percy

    Diterbitkan 2023-09-01
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