Showing 1 - 4 results of 4 for search 'Katie Golden', query time: 0.03s Refine Results
  1. 1
    P471: Quad whole genome sequencing detects reciprocal copy number variants in affected siblings, consistent with familial translocation

    P471: Quad whole genome sequencing detects reciprocal copy number variants in affected siblings, consistent with familial translocation by Katie Golden-Grant, Amanda Buchanan, Alison Coffey, Yvonne Brew, Brittany Thomas, Akanchha Kesari, Denise Perry, Ryan Taft

    Published 2023-01-01
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  2. 2
    Missed diagnoses: Clinically relevant lessons learned through medical mysteries solved by the Undiagnosed Diseases Network

    Missed diagnoses: Clinically relevant lessons learned through medical mysteries solved by the Undiagnosed Diseases Network by Heidi Cope, Rebecca Spillmann, Jill A. Rosenfeld, Elly Brokamp, Rebecca Signer, Kelly Schoch, Emily Glanton, Jennifer A. Sullivan, Ellen Macnamara, Sharyn Lincoln, Katie Golden‐Grant, Undiagnosed Diseases Network, James P. Orengo, Gary Clark, Lindsay C. Burrage, Jennifer E. Posey, Jaya Punetha, Amy Robertson, Joy Cogan, John A. Phillips III, Julian Martinez‐Agosto, Vandana Shashi

    Published 2020-10-01
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  3. 3
    Developing consensus on core outcome sets of domains for acute, the transition from acute to chronic, recurrent/episodic, and chronic pain: results of the INTEGRATE-pain Delphi processResearch in context

    Developing consensus on core outcome sets of domains for acute, the transition from acute to chronic, recurrent/episodic, and chronic pain: results of the INTEGRATE-pain Delphi pro... by Giulia Bova, Anthony Domenichiello, Janelle E. Letzen, Daniela C. Rosenberger, Andrew Siddons, Ulrike Kaiser, Adam Anicich, Ralf Baron, Judy Birch, Didier Bouhassira, George Casey, Katie Golden, Smriti Iyengar, Barbara I. Karp, Hiltrud Liedgens, Winfried Meissner, Kate Nicholson, Leah Pogorzala, Deirdre Ryan, Rolf-Detlef Treede, Peter Tugwell, Dennis C. Turk, Katy Vincent, Jan Vollert, Paula R. Williamson, Sarah A. Woller, Ruth Zaslansky, Laura D. Wandner, Esther M. Pogatzki-Zahn

    Published 2023-12-01
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  4. 4
    Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts

    Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts by Elizabeth E. Blue, Samuel J. Huang, Alyna Khan, Katie Golden-Grant, Brenna Boyd, Elisabeth A. Rosenthal, Madelyn A. Gillentine, Leah R. Fleming, David R. Adams, Lynne Wolfe, Aimee Allworth, Michael J. Bamshad, Nikeisha J. Caruana, Sirisak Chanprasert, Jingheng Chen, Nitsuh Dargie, Daniel Doherty, Marisa W. Friederich, Fuki M. Hisama, Martha Horike-Pyne, Jessica C. Lee, Tonia E. Donovan, Daniella H. Hock, Kathleen A. Leppig, Danny E. Miller, Ghayda Mirzaa, Jane Ranchalis, Wendy H. Raskind, Cole R. Michel, Richard Reisdorph, Ulrike Schwarze, Sam Sheppeard, Samuel Strohbehn, David A. Stroud, Virginia P. Sybert, Mark H. Wener, Andrew B. Stergachis, Christina T. Lam, Gail P. Jarvik, Katrina M. Dipple, Johan L.K. Van Hove, Ian A. Glass

    Published 2024-01-01
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