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2. Treatment and long-term follow-up of distichiasis, with special reference to the Friesian horse: a case series. Hermans H; Ensink JM Equine Vet J; 2014 Jul; 46(4):458-62. PubMed ID: 23927412 [TBL] [Abstract][Full Text] [Related]
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4. A nonsense mutation in B3GALNT2 is concordant with hydrocephalus in Friesian horses. Ducro BJ; Schurink A; Bastiaansen JW; Boegheim IJ; van Steenbeek FG; Vos-Loohuis M; Nijman IJ; Monroe GR; Hellinga I; Dibbits BW; Back W; Leegwater PA BMC Genomics; 2015 Oct; 16():761. PubMed ID: 26452345 [TBL] [Abstract][Full Text] [Related]
5. Genome-wide SNP association-based localization of a dwarfism gene in Friesian dwarf horses. Orr N; Back W; Gu J; Leegwater P; Govindarajan P; Conroy J; Ducro B; Van Arendonk JA; MacHugh DE; Ennis S; Hill EW; Brama PA Anim Genet; 2010 Dec; 41 Suppl 2():2-7. PubMed ID: 21070269 [TBL] [Abstract][Full Text] [Related]
6. A missense mutation in damage-specific DNA binding protein 2 is a genetic risk factor for limbal squamous cell carcinoma in horses. Bellone RR; Liu J; Petersen JL; Mack M; Singer-Berk M; Drögemüller C; Malvick J; Wallner B; Brem G; Penedo MC; Lassaline M Int J Cancer; 2017 Jul; 141(2):342-353. PubMed ID: 28425625 [TBL] [Abstract][Full Text] [Related]
7. A chromosomal region on ECA13 is associated with maxillary prognathism in horses. Signer-Hasler H; Neuditschko M; Koch C; Froidevaux S; Flury C; Burger D; Leeb T; Rieder S PLoS One; 2014; 9(1):e86607. PubMed ID: 24466169 [TBL] [Abstract][Full Text] [Related]
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9. Equine vitiligo-like depigmentation in grey horses is related to genes involved in immune response and tumor metastasis. Druml T; Brem G; Velie B; Lindgren G; Horna M; Ricard A; Grilz-Seger G BMC Vet Res; 2021 Oct; 17(1):336. PubMed ID: 34696794 [TBL] [Abstract][Full Text] [Related]
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13. 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; 49(1):85. PubMed ID: 29141579 [TBL] [Abstract][Full Text] [Related]
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18. Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse. Hack YL; Crabtree EE; Avila F; Sutton RB; Grahn R; Oh A; Gilger B; Bellone RR Equine Vet J; 2021 Mar; 53(2):316-323. PubMed ID: 32654228 [TBL] [Abstract][Full Text] [Related]
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20. Detection of copy number variants in the horse genome and examination of their association with recurrent laryngeal neuropathy. Dupuis MC; Zhang Z; Durkin K; Charlier C; Lekeux P; Georges M Anim Genet; 2013 Apr; 44(2):206-8. PubMed ID: 22582820 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]