Found: 2

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  • Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

    Published in:
    Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-29
    By:
    • Worthey, Elizabeth A.;
    • Raca, Gordana;
    • Laffin, Jennifer J.;
    • Wilk, Brandon M.;
    • Harris, Jeremy M.;
    • Jakielski, Kathy J.;
    • Dimmock, David P.;
    • Strand, Edythe A.;
    • Shriberg, Lawrence D.
    Publication type:
    Article

  • VarSight: prioritizing clinically reported variants with binary classification algorithms.

    Published in:
    BMC Bioinformatics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12859-019-3026-8
    By:
    • Holt, James M.;
    • Wilk, Brandon;
    • Birch, Camille L.;
    • Brown, Donna M.;
    • Gajapathy, Manavalan;
    • Moss, Alexander C.;
    • Sosonkina, Nadiya;
    • Wilk, Melissa A.;
    • Anderson, Julie A.;
    • Harris, Jeremy M.;
    • Kelly, Jacob M.;
    • Shaterferdosian, Fariba;
    • Uno-Antonison, Angelina E.;
    • Weborg, Arthur;
    • Undiagnosed Diseases Network;
    • Acosta, Maria T.;
    • Adam, Margaret;
    • Adams, David R.;
    • Agrawal, Pankaj B.;
    • Alejandro, Mercedes E.
    Publication type:
    Article