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Journal of Animal Science
|
November 7, 2003
Effect of fish meal supplementation on plasma and endometrial fatty acid composition in nonlactating beef cows
P D Burns, T E Engle, M A Harris, et al.
Journal of Animal Science
|
July 9, 2018
Evaluation of moderate to high elevation effects on pulmonary arterial pressure measures in Angus cattle1
Rachel C Pauling, Scott E Speidel, Milton G Thomas, et al.
Journal of Pediatric Hematology/Oncology
|
July 1, 2009
Hypoplastic glomerulocystic kidney disease and hepatoblastoma: a potential association not caused by mutations in hepatocyte nuclear factor 1beta
Omar A Abdul-Rahman, Emma L Edghill, Andrea Kwan, et al.
American Journal of Medical Genetics. Part A
|
May 20, 2018
Current clinical evidence does not support a link between TBL1XR1 and Rett syndrome: Description of one patient with Rett features and a novel mutation in TBL1XR1, and a review of TBL1XR1 phenotypes
Manar Zaghlula, Daniel G Glaze, Gregory M Enns, et al.
Animal Genetics
|
September 12, 2009
Quantitative trait loci with effects on feed efficiency traits in Hereford x composite double backcross populations
G C Márquez, R M Enns, M D Grosz, et al.
Mitochondrion
|
October 11, 2011
Leigh syndrome caused by a novel m.4296G>A mutation in mitochondrial tRNA isoleucine
Rachel Cox, Julia Platt, Li Chieh Chen, et al.
Journal of Animal Science
|
November 30, 2016
Heritabilities and genetic correlations of pulmonary arterial pressure and performance traits in Angus cattle at high altitude
N F Crawford, M G Thomas, T N Holt, et al.
Journal of Animal Science
|
October 7, 2015
Mean pulmonary arterial pressures in Angus steers increase from cow-calf to feedlot-finishing phases
J M Neary, F B Garry, T N Holt, et al.
Pediatric Neurology
|
January 17, 2015
Identification of HIBCH gene mutations causing autosomal recessive Leigh syndrome: a gene involved in valine metabolism
Claudia Soler-Alfonso, Gregory M Enns, Mary Kay Koenig, et al.
Molecular Genetics and Metabolism
|
October 9, 2021
Diagnostic challenges and disease management in patients with a mild Zellweger spectrum disorder phenotype
Gregory M Enns, Zineb Ammous, Ryan W Himes, et al.
Page
of 21
Search research articles
Search
Showing results (61-70 of 208) with videos related to
Sort By:
Page
of 21
Journal of Animal Science
|
November 7, 2003
Effect of fish meal supplementation on plasma and endometrial fatty acid composition in nonlactating beef cows
P D Burns, T E Engle, M A Harris, et al.
Journal of Animal Science
|
July 9, 2018
Evaluation of moderate to high elevation effects on pulmonary arterial pressure measures in Angus cattle1
Rachel C Pauling, Scott E Speidel, Milton G Thomas, et al.
Journal of Pediatric Hematology/Oncology
|
July 1, 2009
Hypoplastic glomerulocystic kidney disease and hepatoblastoma: a potential association not caused by mutations in hepatocyte nuclear factor 1beta
Omar A Abdul-Rahman, Emma L Edghill, Andrea Kwan, et al.
American Journal of Medical Genetics. Part A
|
May 20, 2018
Current clinical evidence does not support a link between TBL1XR1 and Rett syndrome: Description of one patient with Rett features and a novel mutation in TBL1XR1, and a review of TBL1XR1 phenotypes
Manar Zaghlula, Daniel G Glaze, Gregory M Enns, et al.
Animal Genetics
|
September 12, 2009
Quantitative trait loci with effects on feed efficiency traits in Hereford x composite double backcross populations
G C Márquez, R M Enns, M D Grosz, et al.
Mitochondrion
|
October 11, 2011
Leigh syndrome caused by a novel m.4296G>A mutation in mitochondrial tRNA isoleucine
Rachel Cox, Julia Platt, Li Chieh Chen, et al.
Journal of Animal Science
|
November 30, 2016
Heritabilities and genetic correlations of pulmonary arterial pressure and performance traits in Angus cattle at high altitude
N F Crawford, M G Thomas, T N Holt, et al.
Journal of Animal Science
|
October 7, 2015
Mean pulmonary arterial pressures in Angus steers increase from cow-calf to feedlot-finishing phases
J M Neary, F B Garry, T N Holt, et al.
Pediatric Neurology
|
January 17, 2015
Identification of HIBCH gene mutations causing autosomal recessive Leigh syndrome: a gene involved in valine metabolism
Claudia Soler-Alfonso, Gregory M Enns, Mary Kay Koenig, et al.
Molecular Genetics and Metabolism
|
October 9, 2021
Diagnostic challenges and disease management in patients with a mild Zellweger spectrum disorder phenotype
Gregory M Enns, Zineb Ammous, Ryan W Himes, et al.
Page
of 21