Hasil Pencarian - Linlea Armstrong

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  1. 1
    The Identification of Lynch Syndrome in British Columbia

    The Identification of Lynch Syndrome in British Columbia oleh Carol M Cremin, Linlea Armstrong, Sharlene Gill, David Huntsman, Chris Bajdik

    Diterbitkan 2009-01-01
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  2. 2
    Expanding the genotype-phenotype spectrum in SCN8A-related disorders

    Expanding the genotype-phenotype spectrum in SCN8A-related disorders oleh Malavika Hebbar, Nawaf Al-Taweel, Inderpal Gill, Cyrus Boelman, Richard A. Dean, Samuel J. Goodchild, Janette Mezeyova, Noah Gregory Shuart, J. P. Johnson, James Lee, Aspasia Michoulas, Linda L. Huh, Linlea Armstrong, Mary B. Connolly, Michelle K. Demos

    Diterbitkan 2024-01-01
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  3. 3
    Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability

    Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability oleh Farah R. Zahir, Jill C. Mwenifumbo, Hye-Jung E. Chun, Emilia L. Lim, Clara D. M. Van Karnebeek, Madeline Couse, Karen L. Mungall, Leora Lee, Nancy Makela, Linlea Armstrong, Cornelius F. Boerkoel, Sylvie L. Langlois, Barbara M. McGillivray, Steven J. M. Jones, Jan M. Friedman, Marco A. Marra

    Diterbitkan 2017-05-01
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  4. 4
    The practice of genomic medicine: A delineation of the process and its governing principles

    The practice of genomic medicine: A delineation of the process and its governing principles oleh Julia Handra, Julia Handra, Adrienne Elbert, Adrienne Elbert, Nour Gazzaz, Nour Gazzaz, Nour Gazzaz, Nour Gazzaz, Ashley Moller-Hansen, Ashley Moller-Hansen, Stephanie Hyunh, Stephanie Hyunh, Hyun Kyung Lee, Hyun Kyung Lee, Pierre Boerkoel, Emily Alderman, Emily Alderman, Erin Anderson, Erin Anderson, Lorne Clarke, Lorne Clarke, Sara Hamilton, Sara Hamilton, Ronnalea Hamman, Shevaun Hughes, Simon Ip, Sylvie Langlois, Sylvie Langlois, Mary Lee, Laura Li, Frannie Mackenzie, Millan S. Patel, Millan S. Patel, Leah M. Prentice, Karan Sangha, Karan Sangha, Laura Sato, Kimberly Seath, Kimberly Seath, Margaret Seppelt, Anne Swenerton, Anne Swenerton, Lynn Warnock, Jessica L. Zambonin, Jessica L. Zambonin, Cornelius F. Boerkoel, Cornelius F. Boerkoel, Hui-Lin Chin, Hui-Lin Chin, Hui-Lin Chin, Linlea Armstrong, Linlea Armstrong

    Diterbitkan 2023-01-01
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  5. 5
    P531: Developing the patient-reported Genetic testing Utility InDEx (P-GUIDE): Assessing value of genetic testing from patients’ perspectives in multiple clinical contexts

    P531: Developing the patient-reported Genetic testing Utility InDEx (P-GUIDE): Assessing value of genetic testing from patients’ perspectives in multiple clinical contexts oleh Elise Poole, Stephanie Luca, Daniel Assamad, Bowen Xiao, Joyce Yan, Pooja Banglorewala, Cheryl Xia, Wendy Ungar, Lesleigh Abbott, Linlea Armstrong, Patricia Birch, Kym Boycott, June Carroll, Lauren Chad, David Chitayat, Avram Denburg, Rebecca Deyell, Alison Elliott, Catherine Goudie, Anne-Marie Laberge, Melissa Maio, Iskra Peltekova, Becky Quinlan, Sarah Sawyer, Rachel Silver, Maureen Smith, Ronni Teitelbaum, Anita Villani, Tasha Wainstein, Robin Hayeems

    Diterbitkan 2024-01-01
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  6. 6
    Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers

    Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers oleh Rebecca J. Deyell, Yaoqing Shen, Emma Titmuss, Katherine Dixon, Laura M. Williamson, Erin Pleasance, Jessica M. T. Nelson, Sanna Abbasi, Martin Krzywinski, Linlea Armstrong, Melika Bonakdar, Carolyn Ch’ng, Eric Chuah, Chris Dunham, Alexandra Fok, Martin Jones, Anna F. Lee, Yussanne Ma, Richard A. Moore, Andrew J. Mungall, Karen L. Mungall, Paul C. Rogers, Kasmintan A. Schrader, Alice Virani, Kathleen Wee, Sean S. Young, Yongjun Zhao, Steven J. M. Jones, Janessa Laskin, Marco A. Marra, Shahrad R. Rassekh

    Diterbitkan 2024-05-01
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  7. 7
    Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study

    Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study oleh Alison M. Elliott, Shelin Adam, Christèle du Souich, Anna Lehman, Tanya N. Nelson, Clara van Karnebeek, Emily Alderman, Linlea Armstrong, Gudrun Aubertin, Katherine Blood, Cyrus Boelman, Cornelius Boerkoel, Karla Bretherick, Lindsay Brown, Chieko Chijiwa, Lorne Clarke, Madeline Couse, Susan Creighton, Abby Watts-Dickens, William T. Gibson, Harinder Gill, Maja Tarailo-Graovac, Sara Hamilton, Harindar Heran, Gabriella Horvath, Lijia Huang, Gurdip K. Hulait, David Koehn, Hyun Kyung Lee, Suzanne Lewis, Elena Lopez, Kristal Louie, Karen Niederhoffer, Allison Matthews, Kirsten Meagher, Junran J. Peng, Millan S. Patel, Simone Race, Phillip Richmond, Rosemarie Rupps, Ramona Salvarinova, Kimberly Seath, Kathryn Selby, Michelle Steinraths, Sylvia Stockler, Kaoru Tang, Christine Tyson, Margot van Allen, Wyeth Wasserman, Jill Mwenifumbo, Jan M. Friedman

    Diterbitkan 2022-07-01
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