Ling T Guo

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 7

Top Topics

Tyrosine Kinase

Muscular Dystrophy

Top Venues

Journal of veterinary internal medicine

Animal genetics

This page only lists publications with an associated author ORCID identifier.

Publications

G Diane Shelton, Fabrizio Tucciarone, Ling T Guo, Lyndon M Coghill, Leslie A Lyons
Precision medicine using whole genome sequencing identifies a novel dystrophin (DMD) variant for X-linked muscular dystrophy in a cat. Journal of veterinary internal medicine 38 (1) (2024)
G Diane Shelton, Fabrizio Tucciarone, Ling T Guo, Lyndon M Coghill, Leslie A Lyons
Precision medicine using whole genome sequencing identifies a novel dystrophin (DMD) variant for X-linked muscular dystrophy in a cat. Journal of veterinary internal medicine 38 (1) (2024)
G Diane Shelton, Fabrizio Tucciarone, Ling T Guo, Lyndon M Coghill, Leslie A Lyons
Precision medicine using whole genome sequencing identifies a novel dystrophin (DMD) variant for X-linked muscular dystrophy in a cat. Journal of veterinary internal medicine (2024)
Mario Van Poucke, Liesbet Ledeganck, Ling T Guo, G Diane Shelton, Sofie F M Bhatti, Ine Cornelis, Luc Peelman
Exonisation of an intronic L1 element in the dystrophin gene associated with X-linked muscular dystrophy in a Border Collie dog. Animal genetics (2024)
G Diane Shelton, Fabrizio Tucciarone, Ling T Guo, Lyndon M Coghill, Leslie A Lyons
Precision medicine using whole genome sequencing identifies a novel dystrophin (DMD) variant for X-linked muscular dystrophy in a cat. Journal of veterinary internal medicine 38 (1) (2024)
G Diane Shelton, Katie M Minor, Stephanie Thomovsky, Ling T Guo, Steven G Friedenberg, Jonah N Cullen, James R Mickelson
Congenital muscular dystrophy in a dog with a LAMA2 gene deletion. Journal of veterinary internal medicine (2021)
Matthias Christen, Victoria Indzhova, Ling T Guo, Vidhya Jagannathan, Tosso Leeb, G Diane Shelton, Josep Brocal
LAMA2 Nonsense Variant in an Italian Greyhound with Congenital Muscular Dystrophy. Genes 12 (11) (2021)