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Animals : an Open Access Journal From MDPI|March 13, 2024
Variants in CLCN1 and PDE4C Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French BulldogsG Diane Shelton, James R Mickelson, Steven G Friedenberg, et al.Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|June 18, 2013
Unexplained gastrointestinal symptoms: think mitochondrial diseaseThomas P Chapman, Gina Hadley, Carl Fratter, et al.Genes|August 26, 2022
An EHPB1L1 Nonsense Mutation Associated with Congenital Dyserythropoietic Anemia and Polymyopathy in Labrador Retriever LittermatesG Diane Shelton, Katie M Minor, Ling T Guo, et al.Journal of Veterinary Internal Medicine|September 14, 2023
Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich-like congenital muscular dystrophyLeanne Jankelunas, Vishal D Murthy, Annie V Chen, et al.Neuromuscular Disorders : NMD|August 30, 2022
Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotypeG Diane Shelton, Katie M Minor, Natassia M Vieira, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 14, 2004
Hyperconvolution of the inner limiting membrane in vitreomaculopathiesD R J Snead, N Cullen, S James, et al.Genes|January 8, 2025
Biliverdinuria Caused by Exonic BLVRA Deletions in Two Dogs with Green UrineEva Furrow, Jade A Peralta, A Russell Moore, et al.Journal of Veterinary Internal Medicine|February 26, 2026
Autoimmune lymphoproliferative syndrome in Boerboel dogs: clinicopathologic, diagnostic, and genetic characterizationLinda J Tong, Steven G Friedenberg, Jonah N Cullen, et al.Genes|February 24, 2024
Sequence Analysis of Six Candidate Genes in Miniature Schnauzers with Primary HypertriglyceridemiaNicole M Tate, Michaela Underwood, Alison Thomas-Hollands, et al.Neuromuscular Disorders : NMD|July 3, 2023
Canine models of Charcot-Marie-Tooth: MTMR2, MPZ, and SH3TC2 variants in golden retrievers with congenital hypomyelinating polyneuropathyShawna Cook, Blair N Hooser, D Colette Williams, et al.Pageof 6