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PUBMED FOR HANDHELDS

Journal Abstract Search


125 related items for PubMed ID: 34666370

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  • 7. Equine Multiple Congenital Ocular Anomalies (MCOA) syndrome in PMEL17 (Silver) mutant ponies: five cases.
    Komáromy AM, Rowlan JS, La Croix NC, Mangan BG.
    Vet Ophthalmol; 2011 Sep; 14(5):313-20. PubMed ID: 21929608
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  • 8. Targeted analysis of four breeds narrows equine Multiple Congenital Ocular Anomalies locus to 208 kilobases.
    Andersson LS, Lyberg K, Cothran G, Ramsey DT, Juras R, Mikko S, Ekesten B, Ewart S, Lindgren G.
    Mamm Genome; 2011 Jun; 22(5-6):353-60. PubMed ID: 21465164
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  • 9. Ultrasonographic features of PMEL17 (Silver) mutant gene-associated multiple congenital ocular anomalies (MCOA) in Comtois and Rocky Mountain horses.
    Ségard EM, Depecker MC, Lang J, Gemperli A, Cadoré JL.
    Vet Ophthalmol; 2013 Nov; 16(6):429-35. PubMed ID: 23278951
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  • 11. Platinum coat color in red fox (Vulpes vulpes) is caused by a mutation in an autosomal copy of KIT.
    Johnson JL, Kozysa A, Kharlamova AV, Gulevich RG, Perelman PL, Fong HW, Vladimirova AV, Oskina IN, Trut LN, Kukekova AV.
    Anim Genet; 2015 Apr; 46(2):190-9. PubMed ID: 25662789
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  • 13. Explicit evidence for a missense mutation in exon 4 of SLC45A2 gene causing the pearl coat dilution in horses.
    Sevane N, Sanz CR, Dunner S.
    Anim Genet; 2019 Jun; 50(3):275-278. PubMed ID: 30968968
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  • 15. An epistatic effect of KRT25 on SP6 is involved in curly coat in horses.
    Thomer A, Gottschalk M, Christmann A, Naccache F, Jung K, Hewicker-Trautwein M, Distl O, Metzger J.
    Sci Rep; 2018 Apr 23; 8(1):6374. PubMed ID: 29686323
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  • 16. A missense variant in the coil1A domain of the keratin 25 gene is associated with the dominant curly hair coat trait (Crd) in horse.
    Morgenthaler C, Diribarne M, Capitan A, Legendre R, Saintilan R, Gilles M, Esquerré D, Juras R, Khanshour A, Schibler L, Cothran G.
    Genet Sel Evol; 2017 Nov 15; 49(1):85. PubMed ID: 29141579
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  • 17. Frequency of gray coat color in native Chinese horse breeds.
    Gao KX, Chen NB, Liu WJ, Li R, Lan XY, Chen H, Lei CZ, Dang RH.
    Genet Mol Res; 2015 Oct 30; 14(4):14144-50. PubMed ID: 26535731
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