Hasil Pencarian - Alison L Ruhe

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  1. 1
    Partial deletion of the sulfate transporter SLC13A1 is associated with an osteochondrodysplasia in the Miniature Poodle breed.

    Partial deletion of the sulfate transporter SLC13A1 is associated with an osteochondrodysplasia in the Miniature Poodle breed. oleh Mark W Neff, John S Beck, Julie M Koeman, Elissa Boguslawski, Lisa Kefene, Andrew Borgman, Alison L Ruhe

    Diterbitkan 2012-01-01
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  2. 2
    Early onset adult deafness in the Rhodesian Ridgeback dog is associated with an in-frame deletion in the EPS8L2 gene.

    Early onset adult deafness in the Rhodesian Ridgeback dog is associated with an in-frame deletion in the EPS8L2 gene. oleh Takeshi Kawakami, Vandana Raghavan, Alison L Ruhe, Meghan K Jensen, Ausra Milano, Thomas C Nelson, Adam R Boyko

    Diterbitkan 2022-01-01
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  3. 3
    Variation in genes related to cochlear biology is strongly associated with adult-onset deafness in border collies.

    Variation in genes related to cochlear biology is strongly associated with adult-onset deafness in border collies. oleh Jennifer S Yokoyama, Ernest T Lam, Alison L Ruhe, Carolyn A Erdman, Kathryn R Robertson, Aubrey A Webb, D Colette Williams, Melanie L Chang, Marjo K Hytönen, Hannes Lohi, Steven P Hamilton, Mark W Neff

    Diterbitkan 2012-09-01
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  4. 4
    An ADAMTSL2 founder mutation causes Musladin-Lueke Syndrome, a heritable disorder of beagle dogs, featuring stiff skin and joint contractures.

    An ADAMTSL2 founder mutation causes Musladin-Lueke Syndrome, a heritable disorder of beagle dogs, featuring stiff skin and joint contractures. oleh Hannah L Bader, Alison L Ruhe, Lauren W Wang, Aaron K Wong, Kari F Walsh, Rebecca A Packer, Jonathan Mitelman, Kathryn R Robertson, Dennis P O'Brien, Karl W Broman, G Diane Shelton, Suneel S Apte, Mark W Neff

    Diterbitkan 2010-09-01
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