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Journal Abstract Search

185 related items for PubMed ID: 24086599

  • 1. Equine multiple congenital ocular anomalies and silver coat colour result from the pleiotropic effects of mutant PMEL.
    Andersson LS, Wilbe M, Viluma A, Cothran G, Ekesten B, Ewart S, Lindgren G.
    PLoS One; 2013; 8(9):e75639. PubMed ID: 24086599
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  • 2. Multiple congenital ocular anomalies in Icelandic horses.
    Andersson LS, Axelsson J, Dubielzig RR, Lindgren G, Ekesten B.
    BMC Vet Res; 2011 May 26; 7():21. PubMed ID: 21615885
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  • 6. 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 26; 14(5):313-20. PubMed ID: 21929608
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  • 8. Multiple Congenital Ocular Anomalies in a silver coat Missouri Fox Trotter stallion.
    Herb VM, Zehetner V, Blohm KO.
    Tierarztl Prax Ausg G Grosstiere Nutztiere; 2021 Oct 26; 49(5):350-354. PubMed ID: 34666370
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  • 10. A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung disease.
    Metallinos DL, Bowling AT, Rine J.
    Mamm Genome; 1998 Jun 26; 9(6):426-31. PubMed ID: 9585428
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  • 11. A missense mutation in damage-specific DNA binding protein 2 is a genetic risk factor for ocular squamous cell carcinoma in Belgian horses.
    Knickelbein KE, Lassaline ME, Singer-Berk M, Reilly CM, Clode AB, Famula TR, Michau TM, Bellone RR.
    Equine Vet J; 2020 Jan 26; 52(1):34-40. PubMed ID: 30903710
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  • 12. 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 26; 50(3):275-278. PubMed ID: 30968968
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  • 13. A Genome-Wide Association Analysis in Noriker Horses Identifies a SNP Associated With Roan Coat Color.
    Grilz-Seger G, Reiter S, Neuditschko M, Wallner B, Rieder S, Leeb T, Jagannathan V, Mesarič M, Cotman M, Pausch H, Lindgren G, Velie B, Horna M, Brem G, Druml T.
    J Equine Vet Sci; 2020 May 26; 88():102950. PubMed ID: 32303326
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  • 15. Association between population structure and allele frequencies of the glycogen synthase 1 mutation in the Austrian Noriker draft horse.
    Druml T, Grilz-Seger G, Neuditschko M, Brem G.
    Anim Genet; 2017 Feb 26; 48(1):108-112. PubMed ID: 27476720
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  • 20. The horse homolog of congenital aniridia conforms to codominant inheritance.
    Ewart SL, Ramsey DT, Xu J, Meyers D.
    J Hered; 2000 Feb 26; 91(2):93-8. PubMed ID: 10768120
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