Works matching AU Dalton, Joline C.

Results: 3
    1

    Spectrin mutations cause spinocerebellar ataxia type 5.

    Published in:
    Nature Genetics, 2006, v. 38, n. 2, p. 184, doi. 10.1038/ng1728
    By:
    • Ikeda, Yoshio;
    • Dick, Katherine A.;
    • Weatherspoon, Marcy R.;
    • Gincel, Dan;
    • Armbrust, Karen R.;
    • Dalton, Joline C.;
    • Stevanin, Giovanni;
    • Dürr, Alexandra;
    • Zühlke, Christine;
    • Bürk, Katrin;
    • Clark, H. Brent;
    • Brice, Alexis;
    • Rothstein, Jeffrey D.;
    • Schut, Lawrence J.;
    • Day, John W.;
    • Ranum, Laura P. W.
    Publication type:
    Article
    2

    Determining Cost-Optimal Next-Generation Sequencing Panels for Rare Disease and Pharmacogenomics Testing.

    Published in:
    Clinical Chemistry, 2021, v. 67, n. 8, p. 1122, doi. 10.1093/clinchem/hvab059
    By:
    • Katragadda, Shanmukh;
    • Hall, Taryn O.;
    • Bettadapura, Radhakrishna;
    • Dalton, Joline C.;
    • Ganapathy, Aparna;
    • Ghana, Pallavi;
    • Hariharan, Ramesh;
    • Janakiraman, Anand;
    • Kotha, Kumar B. V. S. S. P.;
    • Manjunath, Ashwini;
    • Mannan, Ashraf U.;
    • Niveditha M. S.;
    • Saraf, Shradha;
    • Tzeng, Kathy T. H.;
    • Veeramachanenia, Vamsi
    Publication type:
    Article
    3

    SNP Haplotype Mapping in a Small ALS Family.

    Published in:
    PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005687
    By:
    • Krueger, Katherine A. Dick;
    • Tsuji, Shoji;
    • Fukuda, Yoko;
    • Takahashi, Yuji;
    • Goto, Jun;
    • Mitsui, Jun;
    • Ishiura, Hiroyuki;
    • Dalton, Joline C.;
    • Miller, Michael B.;
    • Day, John W.;
    • Ranum, Laura P. W.
    Publication type:
    Article