Hasil Pencarian - Eric Rush

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  1. 1
    Genetically Targeted Dipeptidyl Peptidase-4 Inhibitor Use in a Patient with a Novel Mutation of MODY type 4

    Genetically Targeted Dipeptidyl Peptidase-4 Inhibitor Use in a Patient with a Novel Mutation of MODY type 4 oleh Christian Mangrum, Eric Rush, Vijay Shivaswamy

    Diterbitkan 2015-01-01
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  2. 2
    Genetically Targeted Dipeptidyl Peptidase-4 Inhibitor Use in a Patient with a Novel Mutation of MODY type 4

    Genetically Targeted Dipeptidyl Peptidase-4 Inhibitor Use in a Patient with a Novel Mutation of MODY type 4 oleh Christian Mangrum, Eric Rush, Vijay Shivaswamy

    Diterbitkan 2015-10-01
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  3. 3
    P629: A novel 198 kb partial duplication in KMT2C: Report of a patient with features of Kleefstra syndrome-2 and adrenal ganglioneuroblastoma

    P629: A novel 198 kb partial duplication in KMT2C: Report of a patient with features of Kleefstra syndrome-2 and adrenal ganglioneuroblastoma oleh Rishabh Gaur, John Herriges, Isabelle Thiffault, Julie Joyce, Eric Rush, Elena Repnikova

    Diterbitkan 2024-01-01
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  4. 4
    P251: XLH molecular diagnoses and the PHEX gene variant landscape: Sponsored hypophosphatemia gene panel testing findings from 2019 vs 2022

    P251: XLH molecular diagnoses and the PHEX gene variant landscape: Sponsored hypophosphatemia gene panel testing findings from 2019 vs 2022 oleh Nicole Miller, Omid Japalaghi, Eric Rush, Kathryn Dahir, Prameela Ramesan, Heather McLaughlin

    Diterbitkan 2023-01-01
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  5. 5
    89 Two Newly Developed Frontiers CTSI Applications to Support Recruitment and Trial Management: The Frontiers Trial Finder Mobile App and a Predictive Accrual Web-based App

    89 Two Newly Developed Frontiers CTSI Applications to Support Recruitment and Trial Management: The Frontiers Trial Finder Mobile App and a Predictive Accrual Web-based App oleh Hanluen Kuo, Vinay Murakonda, Hunter Hines, Dinesh Pal Mudaranthakam, Paula Monaghan-Nichols, Eric Rush, Jeffrey Statland

    Diterbitkan 2024-04-01
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  6. 6
    P551: GATEways to improved test utilization: Opening doors and building bridges

    P551: GATEways to improved test utilization: Opening doors and building bridges oleh Lee Zellmer, Mary Rindler, Maggie Humphrey, Jennifer Roberts, Eric Rush, JD Nolen, John Herriges, Ara Hall, Shivarajan Amudhavalli, Carol Saunders

    Diterbitkan 2023-01-01
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  7. 7
    P398: A rare report of a child with mosaic trisomy 4

    P398: A rare report of a child with mosaic trisomy 4 oleh Lauren Bartik, Elena Repnikova, Eric Rush, Jennifer Roberts, Erin Baldwin, John Carey, Lorenzo Botto, John O'Shea, Ting Wen, Pinar Bayrak-Toydemir, Rong Mao, Undiagnosed Diseases Network, Bonnie Sullivan

    Diterbitkan 2024-01-01
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  8. 8
    P571: Expanding the genetic and phenotypic spectrum of cohesinopathies in a single center

    P571: Expanding the genetic and phenotypic spectrum of cohesinopathies in a single center oleh Isabelle Thiffault, Joseph Alaimo, Vitoria Paolillo, Florencia Del Viso, Ana Cohen, Emily Farrow, Susan Starling, Maggie Humphrey, Caitlin Schwager, Lauren Bartik, Kendra Engleman, Laura Cross, Holly Welsh, Eric Rush, Shivarajan Amudhavalli, Bonnie Sullivan, Dihong Zhou, Elizabeth Shaffer, Waseem Baig, Lee Zellmer, Mary Rindler, Tricia Zion, Emelia Boillat, Tomi Pastinen, Carol Saunders, Isabelle Thiffault

    Diterbitkan 2023-01-01
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