檢索結果 - Scott C. Wildenberg

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  1. 1
    A Second Locus for Familial High Myopia Maps to Chromosome 12q

    A Second Locus for Familial High Myopia Maps to Chromosome 12q 由 Terri L. Young, Shawn M. Ronan, Alison B. Alvear, Scott C. Wildenberg, William S. Oetting, Larry D. Atwood, Douglas J. Wilkin, Richard A. King

    出版 1998
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  2. 2
    Evidence That a Locus for Familial High Myopia Maps to Chromosome 18p

    Evidence That a Locus for Familial High Myopia Maps to Chromosome 18p 由 Terri L. Young, Shawn M. Ronan, Leslie A. Drahozal, Scott C. Wildenberg, Alison B. Alvear, William S. Oetting, Larry D. Atwood, Douglas J. Wilkin, Richard A. King

    出版 1998
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  3. 3
    New Locus for Autosomal Dominant High Myopia Maps to the Long Arm of Chromosome 17

    New Locus for Autosomal Dominant High Myopia Maps to the Long Arm of Chromosome 17 由 Prasuna Paluru, Shawn M. Ronan, Elise Héon, Marcella Devoto, Scott C. Wildenberg, Genaro S. Scavello, Ann M. Holleschau, Outi Ma ̈kitie, William G. Cole, Richard A. King, Terri L. Young

    出版 2003
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    The mouse pale ear ( <i>ep</i> ) mutation is the homologue of human Hermansky–Pudlak syndrome

    The mouse pale ear ( <i>ep</i> ) mutation is the homologue of human Hermansky–Pudlak syndrome 由 John M. Gardner, Scott C. Wildenberg, Natalie M. Keiper, Edward K. Novak, Michael E. Rusiniak, Richard T. Swank, Neelu Puri, Joshua N. Finger, Nobuko Hagiwara, Anne L. Lehman, Tracy L. Gales, M. E. Bayer, Richard A. King, Murray H. Brilliant

    出版 1997
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