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J Trent

Showing results (51-60 of 342) with videos related to

Pageof 35
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Pathology|June 24, 2026
The utility of artificial intelligence for DNA variant curation in the Mendelian genetic disorder familial hypercholesterolaemiaDominic Kaul, Huong Le, Edward Kwan, et al.
Prenatal Diagnosis|May 1, 1990
Exclusion of beta-thalassaemia by biopsy and DNA amplification in mouse pre-embryosR Lindeman, J Lutjen, C O'Neill, et al.
Neuroreport|April 13, 2004
A polymorphism in the poliovirus receptor gene differs in motor neuron diseaseRebecca Saunderson, Bing Yu, Ronald J Trent, et al.
Clinical Genetics|January 10, 2001
Polymorphisms in the CAG repeat--a source of error in Huntington disease DNA testingS Yu, A Fimmel, D Fung, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 1, 1984
Alpha thalassaemia in pregnancyR J Trent, J Yakas, J Black, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 18, 2003
Genetically confirmed clinical Huntington's disease with no observable cell lossM Caramins, G Halliday, E McCusker, et al.
Pathology|October 1, 1985
Antenatal diagnosis of severe beta thalassemia during the first trimester of pregnancyR J Trent, J Anderson, T Boogert, et al.
Vaccine|January 26, 2022
Predictors of pneumococcal vaccination among Australian adults at high risk of pneumococcal diseaseMallory J Trent, Daniel A Salmon, C Raina MacIntyre
American Journal of Clinical Pathology|February 1, 1987
Comparison of Clostridium difficile detection by monolayer and by inhibition of nucleoside uptakeJ E Fuhr, D J Trent, I R Collmann
Journal of Medical Education|February 1, 1982
Evaluation of behavior and development training for pediatric residentsP J Trent, R A Hock, W S Yancy
Pageof 35

Showing results (51-60 of 342) with videos related to

Sort By:
Pageof 35
Pathology|June 24, 2026
The utility of artificial intelligence for DNA variant curation in the Mendelian genetic disorder familial hypercholesterolaemiaDominic Kaul, Huong Le, Edward Kwan, et al.
Prenatal Diagnosis|May 1, 1990
Exclusion of beta-thalassaemia by biopsy and DNA amplification in mouse pre-embryosR Lindeman, J Lutjen, C O'Neill, et al.
Neuroreport|April 13, 2004
A polymorphism in the poliovirus receptor gene differs in motor neuron diseaseRebecca Saunderson, Bing Yu, Ronald J Trent, et al.
Clinical Genetics|January 10, 2001
Polymorphisms in the CAG repeat--a source of error in Huntington disease DNA testingS Yu, A Fimmel, D Fung, et al.
The Australian & New Zealand Journal of Obstetrics & Gynaecology|February 1, 1984
Alpha thalassaemia in pregnancyR J Trent, J Yakas, J Black, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 18, 2003
Genetically confirmed clinical Huntington's disease with no observable cell lossM Caramins, G Halliday, E McCusker, et al.
Pathology|October 1, 1985
Antenatal diagnosis of severe beta thalassemia during the first trimester of pregnancyR J Trent, J Anderson, T Boogert, et al.
Vaccine|January 26, 2022
Predictors of pneumococcal vaccination among Australian adults at high risk of pneumococcal diseaseMallory J Trent, Daniel A Salmon, C Raina MacIntyre
American Journal of Clinical Pathology|February 1, 1987
Comparison of Clostridium difficile detection by monolayer and by inhibition of nucleoside uptakeJ E Fuhr, D J Trent, I R Collmann
Journal of Medical Education|February 1, 1982
Evaluation of behavior and development training for pediatric residentsP J Trent, R A Hock, W S Yancy
Pageof 35