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  1. Ames, Angharad [Author]; Arnold, Hayley S. [Author]; Beal, Deryk [Author]; Beilby, Janet [Author]; Below, Jennifer E. [Author]; Byrd, Courtney [Author]; Choi, Dahye [Author]; Coleman, Craig [Author]; DiLollo, Anthony [Author]; Eggers, Kurt [Author]; Fortier-Blanc, Julie [Author]; Franken, Marie-Christine [Author]; Garbarino, Julianne [Author]; Gerlach-Houck, Hope [Author]; Gillis, Corrin I. [Author]; Hall, Nancy E. [Author]; Hearne, Anna [Author]; Herring, Caryn [Author]; Jackson, Eric S. [Author]; Johnson, Kia Noelle [Author]; Jones, Robin [Author]; Kelly, Ellen M. [Author]; Kraft, Shelly Jo [Author]; LaSalle, Lisa [Author]; [...] ; Zebrowski, Patricia M. [Editor]; Anderson, Julie D. [Editor]; Conture, Edward G. [Editor]

    Stuttering and Related Disorders of Fluency - [4. Edition.]

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    New York: Thieme Medical Publishers, Inc., 2022

  2. Morton, Cynthia C.; Marazita, Mary L.; Peter, Beate; Rice, Mabel L.; Kraft, Shelly Jo; Barkmeier‐Kraemer, Julie; Balaban, Carey; Phillips, Michael; Schoden, Jennifer; Maiese, Deborah; Hendershot, Tabitha; Hamilton, Carol M.

    Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit

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    Wiley, 2022

    Published in: Annals of Human Genetics

  3. Shaw, Douglas M.; Polikowsky, Hannah P.; Pruett, Dillon G.; Chen, Hung-Hsin; Petty, Lauren E.; Viljoen, Kathryn Z.; Beilby, Janet M.; Jones, Robin M.; Kraft, Shelly Jo; Below, Jennifer E.

    Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering

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    Elsevier BV, 2021

    Published in: The American Journal of Human Genetics

  4. Polikowsky, Hannah G.; Shaw, Douglas M.; Petty, Lauren E.; Chen, Hung-Hsin; Pruett, Dillon G.; Linklater, Jonathon P.; Viljoen, Kathryn Z.; Beilby, Janet M.; Highland, Heather M.; Levitt, Brandt; Avery, Christy L.; Mullan Harris, Kathleen; Jones, Robin M.; Below, Jennifer E.; Kraft, Shelly Jo

    Population-based genetic effects for developmental stuttering

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    Elsevier BV, 2022

    Published in: Human Genetics and Genomics Advances