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Showing results (341-350 of 412) with videos related to

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Neurogenetics|February 16, 2005
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegiaJohanna A Reed, Phillip A Wilkinson, Heema Patel, et al.
Magnetic Resonance Annual|January 1, 1985
Principles of magnetic resonanceJ P Jones, C L Partain, M R Mitchell, et al.
ACS Nano|September 1, 2018
Cation-Activated Avidity for Rapid Reconfiguration of DNA NanodevicesAlexander E Marras, Ze Shi, Michael G Lindell, et al.
European Journal of Human Genetics : EJHG|December 31, 1997
Further delineation of the critical region for noonan syndrome on the long arm of chromosome 12A F Brady, C R Jamieson, I van der Burgt, et al.
Journal of Racial and Ethnic Health Disparities|October 7, 2025
Disparities in Stage at Diagnosis and Cancer Progression by Race and Socioeconomic Deprivation: A Pan-Tumor Analysis in the US Community Oncology SettingAndrew J Osterland, Yunfei Wang, Esther R Smith-Howell, et al.
Human Genetics|May 8, 2000
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22A R Afzal, A Rajab, C Fenske, et al.
Orthopaedic Journal of Sports Medicine|March 19, 2021
Sport- and Gender-Based Differences in Head Impact Exposure and Mechanism in High School SportsColin M Huber, Declan A Patton, Catherine C McDonald, et al.
Journal of Human Genetics|February 4, 2005
Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11Kamini Kalidas, Adam C Shaw, Andrew H Crosby, et al.
Nature Genetics|December 1, 1994
Mapping a gene for Noonan syndrome to the long arm of chromosome 12C R Jamieson, I van der Burgt, A F Brady, et al.
The Protein Journal|November 15, 2006
The effects of removing the GAT domain from E. coli GMP synthetaseJessica L Abbott, Jordan M Newell, Christine M Lightcap, et al.
Pageof 42

Showing results (341-350 of 412) with videos related to

Sort By:
Pageof 42
Neurogenetics|February 16, 2005
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegiaJohanna A Reed, Phillip A Wilkinson, Heema Patel, et al.
Magnetic Resonance Annual|January 1, 1985
Principles of magnetic resonanceJ P Jones, C L Partain, M R Mitchell, et al.
ACS Nano|September 1, 2018
Cation-Activated Avidity for Rapid Reconfiguration of DNA NanodevicesAlexander E Marras, Ze Shi, Michael G Lindell, et al.
European Journal of Human Genetics : EJHG|December 31, 1997
Further delineation of the critical region for noonan syndrome on the long arm of chromosome 12A F Brady, C R Jamieson, I van der Burgt, et al.
Journal of Racial and Ethnic Health Disparities|October 7, 2025
Disparities in Stage at Diagnosis and Cancer Progression by Race and Socioeconomic Deprivation: A Pan-Tumor Analysis in the US Community Oncology SettingAndrew J Osterland, Yunfei Wang, Esther R Smith-Howell, et al.
Human Genetics|May 8, 2000
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22A R Afzal, A Rajab, C Fenske, et al.
Orthopaedic Journal of Sports Medicine|March 19, 2021
Sport- and Gender-Based Differences in Head Impact Exposure and Mechanism in High School SportsColin M Huber, Declan A Patton, Catherine C McDonald, et al.
Journal of Human Genetics|February 4, 2005
Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11Kamini Kalidas, Adam C Shaw, Andrew H Crosby, et al.
Nature Genetics|December 1, 1994
Mapping a gene for Noonan syndrome to the long arm of chromosome 12C R Jamieson, I van der Burgt, A F Brady, et al.
The Protein Journal|November 15, 2006
The effects of removing the GAT domain from E. coli GMP synthetaseJessica L Abbott, Jordan M Newell, Christine M Lightcap, et al.
Pageof 42