Hasil Pencarian - Meredith Curtis

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  1. 1
    O47: Leveraging somatic cancer mutation data to predict the pathogenicity of germline missense variants*

    O47: Leveraging somatic cancer mutation data to predict the pathogenicity of germline missense variants* oleh Bushra Haque, Saba Birkadze, Amy Pan, Alice Xu, Meredith Curtis, Gregory Costain

    Diterbitkan 2023-01-01
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  2. 2
    P829: Comparative medical genetics to facilitate the interpretation of rare missense variation

    P829: Comparative medical genetics to facilitate the interpretation of rare missense variation oleh Bushra Haque, George Guirguis, Meredith Curtis, Hera Mohsin, Susan Walker, Michelle Morrow, Gregory Costain

    Diterbitkan 2024-01-01
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  3. 3
    P642: Development and deployment of clinical genome sequencing using a cloud-based platform

    P642: Development and deployment of clinical genome sequencing using a cloud-based platform oleh Lynette Lau, Edward Higginbotham, Wilson Sung, Venuja Sriretnakumar, Meredith Curtis, Caitlin Chisholm, Meredith Gillespie, Anna Pan, Sean Kim, Sean Simko, E. Magda Price, Marianne Eliou, Anna Szuto, Michelle Axford, Martin Somerville, Kym Boycott, Jean McGowan-Jordan, Melaine Beaulieu Bergeron, James Stavropoulos, Lijia Huang, Christian Marshall

    Diterbitkan 2024-01-01
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  4. 4
    P305: Evaluation of the feasibility, diagnostic yield, and utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): An international pilot study

    P305: Evaluation of the feasibility, diagnostic yield, and utility of rapid genome sequencing in infantile epilepsy (Gene-STEPS): An international pilot study oleh Nicole Si Yan Liang, Gregory Costain, Alissa D'Gama, Amy McTague, Katherine Howell, Vann Chau, Sarah Mulhern, Annapurna Poduri, Ingrid Scheffer, Beth Sheidley, Meredith Curtis, Edward Higginbotham, Tayyaba Khan, Lyndsey McRae, Kimberly Wiltrout, Robin Hayeems, Puneet Jain, Sebastian Lunke, Christian Marshall, Lyn Chitty, Shira Rockowitz, Zornitza Stark, Susan White

    Diterbitkan 2024-01-01
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  5. 5
    Seeking American Society of Clinical Oncology‐Quality Oncology Practice Initiative (ASCO‐QOPI) certification in a northern New England rural health system and cancer care network

    Seeking American Society of Clinical Oncology‐Quality Oncology Practice Initiative (ASCO‐QOPI) certification in a northern New England rural health system and cancer care network... oleh Hilary M. Perrey, Evelyn Taylor, Brett F. Cropp, Meaghan J. Bumpus, Shannon Lessard, Jeanette A. Pretorius, Jonathan H. Angus, Megan F. Duperreault, Amanda Snow, Dorothy Wang, Meredith Curtis, Lauren A. Couture, David R. Adolphson, Kimberly Smith, Joy H. Moody, Michael J. Bianchi, Mark G. Parker, Amit Sanyal, Scot C. Remick

    Diterbitkan 2024-07-01
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  6. 6
    P616: Genome-wide Sequencing Ontario (GSO): Insight into Ontario’s rare disease landscape

    P616: Genome-wide Sequencing Ontario (GSO): Insight into Ontario’s rare disease landscape oleh Meredith Gillespie, Robin Hayeems, Christian Marshall, Anna Szuto, Caitlin Chisholm, Wendy Ungar, James Stavropoulos, Lijia Huang, Viji Venkataramanan, Lynette Lau, Wilson Sung, Melanie Beaulieu Bergeron, Ted Higginbotham, Meredith Curtis, Venuja Sriretnakumar, Hassan Zaidi, Emma Hitchcock, Audrey Schaffer, Sarah Sawyer, Wendy Ungar, Gregory Costain, Roberto Mendoza-Londono, Robin Hayeems, Martin Somerville, Kym Boycott, Taila Hartley

    Diterbitkan 2024-01-01
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  7. 7
    P540: Genome-wide Sequencing Ontario (GSO): Canada’s first provincial clinical genome-wide sequencing service

    P540: Genome-wide Sequencing Ontario (GSO): Canada’s first provincial clinical genome-wide sequencing service oleh Meredith Gillespie, Robin Hayeems, Christian Marshall, Anna Szuto, Caitlin Chisholm, James Stavropoulos, Lijia Huang, Lynette Lau, Wilson Sung, Melanie Beaulieu Bergeron, Ted Higginbotham, Meredith Curtis, Venuja Sriretnakumar, Hassan Zaidi, Emma Hitchcock, Audrey Schaffer, Taila Hartley, Sarah Sawyer, Wendy Ungar, Gregory Costain, Roberto Mendoza-Londono, Anna Pan, Jennifer Keating, Diana Matviychuk, Tamara Braid, Niri Carroll, Martin Somerville, Kym Boycott

    Diterbitkan 2024-01-01
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  8. 8
    Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences

    Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences oleh Roozbeh Manshaei, Daniele Merico, Daniele Merico, Miriam S. Reuter, Miriam S. Reuter, Worrawat Engchuan, Bahareh A. Mojarad, Rajiv Chaturvedi, Rajiv Chaturvedi, Tracy Heung, Tracy Heung, Giovanna Pellecchia, Mehdi Zarrei, Mehdi Zarrei, Thomas Nalpathamkalam, Reem Khan, John B. A. Okello, Eriskay Liston, Meredith Curtis, Ryan K. C. Yuen, Ryan K. C. Yuen, Ryan K. C. Yuen, Christian R. Marshall, Christian R. Marshall, Christian R. Marshall, Christian R. Marshall, Rebekah K. Jobling, Rebekah K. Jobling, Erwin Oechslin, Rachel M. Wald, Rachel M. Wald, Candice K. Silversides, Stephen W. Scherer, Stephen W. Scherer, Stephen W. Scherer, Stephen W. Scherer, Raymond H. Kim, Raymond H. Kim, Raymond H. Kim, Anne S. Bassett, Anne S. Bassett, Anne S. Bassett, Anne S. Bassett, Anne S. Bassett

    Diterbitkan 2020-09-01
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