Deletion of 2.7 kb near HOXD3 in an Arabian horse with occipitoatlantoaxial malformation

Por Bordbari, MH, Penedo, MCT, Aleman, M., Valberg, SJ, Mickelson, J., Finno, CJ
Publicado no Anim Genet (2017)

Genetic mapping of recurrent exertional rhabdomyolysis in a population of North American Thoroughbreds

Por Fritz, K.L., McCue, M.E., Valberg, S.J., Rendahl, A.K., Mickelson, J.R.
Publicado em 2012

Concurrent Equine Degenerative Myeloencephalopathy and Equine Motor Neuron Disease in Three Young Horses

Por Finno, C.J., Miller, A.D., Sisó, S., Divers, T., Gianino, G., Barro, M.V., Valberg, S.J.
Publicado no J Vet Intern Med (2016)

Major Histocompatibility Complex I and II Expression and Lymphocytic Subtypes in Muscle of Horses with Immune‐Mediated Myositis

Por Durward‐Akhurst, S.A., Finno, C.J., Barnes, N., Shivers, J., Guo, L.T., Shelton, G.D., Valberg, S.J.
Publicado no J Vet Intern Med (2016)

Suspected Congenital Centronuclear Myopathy in an Arabian‐cross Foal

Por Polle, F., Andrews, F.M., Gillon, T., Eades, S.C., McConnico, R.S., Strain, G.M., Valberg, S.J., Guo, L.T., Shelton, G.D.
Publicado no J Vet Intern Med (2014)

Genome sequence, comparative analysis and population genetics of the domestic horse (Equus caballus)

Por Wade, CM, Giulotto, E, Sigurdsson, S, Zoli, M, Gnerre, S, Imsland, F, Lear, TL, Adelson, DL, Bailey, E, Bellone, RR, Blöcker, H, Distl, O, Edgar, RC, Garber, M, Leeb, T, Mauceli, E, MacLeod, JN, Penedo, MCT, Raison, JM, Sharpe, T, Vogel, J, Andersson, L, Antczak, DF, Biagi, T, Binns, MM, Chowdhary, BP, Coleman, SJ, Della Valle, G, Fryc, S, Guérin, G, Hasegawa, T, Hill, EW, Jurka, J, Kiialainen, A, Lindgren, G, Liu, J, Magnani, E, Mickelson, JR, Murray, J, Nergadze, SG, Onofrio, R, Pedroni, S, Piras, MF, Raudsepp, T, Rocchi, M, Røed, KH, Ryder, OA, Searle, S, Skow, L, Swinburne, JE, Syvänen, AC, Tozaki, T, Valberg, SJ, Vaudin, M, White, JR, Zody, MC, Lander, ES, Lindblad-Toh, K
Publicado em 2009