Hasil Pencarian - Denise L. Perry

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  1. 1
    Disclosing genetic risk for Alzheimer's dementia to individuals with mild cognitive impairment

    Disclosing genetic risk for Alzheimer's dementia to individuals with mild cognitive impairment oleh Kurt D. Christensen, Jason Karlawish, J. Scott Roberts, Wendy R. Uhlmann, Kristin Harkins, Elisabeth M. Wood, Thomas O. Obisesan, Lan Q. Le, L. Adrienne Cupples, Emilie S. Zoltick, Megan S. Johnson, Margaret K. Bradbury, Leo B. Waterston, Clara A. Chen, Sara Feldman, Denise L. Perry, Robert C. Green, for the REVEAL Study Group

    Diterbitkan 2020-01-01
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  2. 2
    Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases

    Reactive gene curation to support interpretation and reporting of a clinical genome test for rare disease: Experience from over 1,000 cases oleh Amanda R. Clause, Julie P. Taylor, Revathi Rajkumar, Krista Bluske, Maren Bennett, Laura M. Amendola, David R. Bentley, Ryan J. Taft, Denise L. Perry, Alison J. Coffey, Carolyn Brown, Matthew P. Brown, Amanda Buchanan, Brendan Burns, Nicole J. Burns, Anjana Chandrasekhar, Aditi Chawla, Katie Golden-Grant, Akanchha Kesari, Alka Malhotra, Becky Milewski, Samin A. Sajan, Zinayida Schlachetzki, Sarah Schmidt, Brittany Thomas, Erin Thorpe

    Diterbitkan 2023-02-01
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  3. 3
    Best practices for the interpretation and reporting of clinical whole genome sequencing

    Best practices for the interpretation and reporting of clinical whole genome sequencing oleh Christina A. Austin-Tse, Vaidehi Jobanputra, Denise L. Perry, David Bick, Ryan J. Taft, Eric Venner, Richard A. Gibbs, Ted Young, Sarah Barnett, John W. Belmont, Nicole Boczek, Shimul Chowdhury, Katarzyna A. Ellsworth, Saurav Guha, Shashikant Kulkarni, Cherisse Marcou, Linyan Meng, David R. Murdock, Atteeq U. Rehman, Elizabeth Spiteri, Amanda Thomas-Wilson, Hutton M. Kearney, Heidi L. Rehm, Medical Genome Initiative*

    Diterbitkan 2022-04-01
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