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Journal Abstract Search

213 related items for PubMed ID: 26059442

  • 1. A novel KIT variant in an Icelandic horse with white-spotted coat colour.
    Haase B, Jagannathan V, Rieder S, Leeb T.
    Anim Genet; 2015 Aug; 46(4):466. PubMed ID: 26059442
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  • 2. Seven novel KIT mutations in horses with white coat colour phenotypes.
    Haase B, Brooks SA, Tozaki T, Burger D, Poncet PA, Rieder S, Hasegawa T, Penedo C, Leeb T.
    Anim Genet; 2009 Oct; 40(5):623-9. PubMed ID: 19456317
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  • 3. Coat Color Roan Shows Association with KIT Variants and No Evidence of Lethality in Icelandic Horses.
    Voß K, Tetens J, Thaller G, Becker D.
    Genes (Basel); 2020 Jun 22; 11(6):. PubMed ID: 32580410
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  • 4. Whole genome sequencing reveals a novel deletion variant in the KIT gene in horses with white spotted coat colour phenotypes.
    Dürig N, Jude R, Holl H, Brooks SA, Lafayette C, Jagannathan V, Leeb T.
    Anim Genet; 2017 Aug 22; 48(4):483-485. PubMed ID: 28444912
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  • 12. De novo mutation of KIT causes extensive coat white patterning in a family of Berber horses.
    Martin K, Patterson Rosa L, Vierra M, Foster G, Brooks SA, Lafayette C.
    Anim Genet; 2021 Feb 22; 52(1):135-137. PubMed ID: 33111383
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  • 13. Haematological parameters are normal in dominant white Franches-Montagnes horses carrying a KIT mutation.
    Haase B, Obexer-Ruff G, Dolf G, Rieder S, Burger D, Poncet PA, Gerber V, Howard J, Leeb T.
    Vet J; 2010 Jun 22; 184(3):315-7. PubMed ID: 19362501
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  • 14. An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds.
    Haase B, Jude R, Brooks SA, Leeb T.
    Anim Genet; 2008 Jun 22; 39(3):306-9. PubMed ID: 18410476
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  • 19. A de novo missense mutation in KIT is responsible for dominant white spotting phenotype in a Standardbred horse.
    Esdaile E, Till B, Kallenberg A, Fremeux M, Bickel L, Bellone RR.
    Anim Genet; 2022 Aug 22; 53(4):534-537. PubMed ID: 35641888
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  • 20. Molecular genetics of coat colour variations in White Galloway and White Park cattle.
    Brenig B, Beck J, Floren C, Bornemann-Kolatzki K, Wiedemann I, Hennecke S, Swalve H, Schütz E.
    Anim Genet; 2013 Aug 22; 44(4):450-3. PubMed ID: 23418861
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