Selective Intestinal Cobalamin Malabsorption with Proteinuria (Imerslund‐Gräsbeck Syndrome) in Juvenile Beagles by Fyfe, J.C, Hemker, S.L, Venta, P.J, Stebbing, B, Giger, U

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SCID in Jack Russell Terriers: A New Animal Model of DNA-PKcs Deficiency by Meek, Katheryn, Kienker, Laura, Dallas, Clarissa, Wang, Wei, Dark, Michael J, Venta, Patrick J, Huie, Maryann L, Hirschhorn, Rochelle, Bell, Tom

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The long and the short of it: evidence that FGF5 is a major determinant of canine 'hair'-itability by Housley, D. J. E., Venta, P. J.

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Congenital ureteral ectopia in continent and incontinent-related Entlebucher Mountain Dogs: 13 cases (2006-2009) by North, C, Kruger, J.M, Venta, P.J, Miller, J.M, Rosenstein, D.S, Randall, E.K, White, B, Fitzgerald, S.D

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Molecular Basis of Human Carbonic Anhydrase II Deficiency by Roth, Donna E., Venta, Patrick J., Tashian, Richard E., Sly, William S.

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A von Willebrand's Factor Genomic Nucleotide Variant and Polymerase Chain Reaction Diagnostic Test Associated with Inheritable Type-2 von Willebrand's Disease in a Line of German S... by Kramer, J. W., Venta, P. J., Klein, S. R., Cao, Y., Schall, W. D., Yuzbasiyan-Gurkan, V.

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N-Ethyl-N-nitrosourea-Induced Null Mutation at the Mouse Car-2 Locus: An Animal Model for Human Carbonic Anhydrase II Deficiency Syndrome by Lewis, Susan E., Erickson, Robert P., Barnett, Lois B., Venta, Patrick J., Tashian, Richard E.

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Within-breed heterozygosity of canine single nucleotide polymorphisms identified by across-breed comparison by Brouillette, J. A., Venta, P. J.

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Carbonic anhydrase II deficiency : single-base deletion in Exon 7 is the predominant mutation in Caribbean hispanic patients by HU, P. Y, ERNST, A. R, SLY, W. S, VENTA, P. J, SKAGGS, L. A, TASHIAN, R. E

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Polymorphism identification within 50 equine gene-specific sequence tagged sites by Shubitowski, D. M., Venta, P. J., Douglass, C. L., Zhou, R.-X., Ewart, S. L.

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Expression of toll-like receptor 2 mRNA in bronchial epithelial cells is not induced in RAO-affected horses by Berndt, A, Derksen, F.J, Venta, P.J, Karmaus, W, Ewart, S, Yuzbasiyan-Gurkan, V, Robinson, N.E

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Mapping of the FES and FURIN genes to porcine chromosome 7 by Ernst, C.W, Raney, N.E, Rilington, V.D, Rohrer, G.A, Brouillette, J.A, Venta, P.J

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A PCR‐RSP Csp6I site in the canine DLA‐DQA1 gene by Venta, P. J., Cao, Y.

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MspI RSP in exon 42 of the canine von Willebrand factor (VWF) gene by Venta, P. J., Vidal, M.

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AIRS-PCR for the canine DLA-DQA1 F141L polymorphism by Venta, P J, Cao, Y

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Mucin genes in horse airways: MUC5AC, but not MUC2, may play a role in recurrent airway obstruction by GERBER, V., ROBINSON, N. E., VENTA, P. J., RAWSON, J., JEFCOAT, A. M., HOTCHKISS, J. A.

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Localization of the mitochondrial carbonic anhydrase V gene, Car5, on mouse chromosome 8 by Lakkis, M M, Venta, P J, Tashian, R E

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canine linkage map: 39 linkage groups by Lingaas, F, Aarskaug, T, Gerlach, J.A, Juneja, R.K, Fredholm, M, Sampson, J, Suter, N, Holmes, N.G, Binns, M.M, Ryder, E.J

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Dinucleotide repeat polymorphism in the canine retinoblastoma (RB1) gene by Venta, P J, Cao, Y, Alexander, L, Yuzbasiyan‐Gurkan, V

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Mutation Creates an Open Reading Frame Within the 5' Untranslated Region of Macaque Erythrocyte Carbonic Anhydrase (CA) I mRNA That Suppresses CA I Expression and Supports the Scan... by Nils C. H. Bergenhem, Venta, Patrick J., Hopkins, Penelope J., Kim, Hyung J., Tashian, Richard E.

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