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C Priestley

Showing results (81-90 of 86) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 20, 2014
Mutation of Plekha7 attenuates salt-sensitive hypertension in the ratBradley T Endres, Jessica R C Priestley, Oleg Palygin, et al.
International Journal of Neonatal Screening|April 25, 2022
Newborn Screening for X-Linked Adrenoleukodystrophy: Review of Data and Outcomes in PennsylvaniaJessica R C Priestley, Laura A Adang, Sarah Drewes Williams, et al.
Molecular Genetics and Metabolism Reports|November 24, 2022
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signatureJessica R C Priestley, Lisa M Pace, Kuntal Sen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 1, 2023
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrumJessica R C Priestley, Ashish R Deshwar, Harsha Murthy, et al.
Pediatrics|June 1, 2022
Clinical Effectiveness of Telemedicine-Based Pediatric Genetics CareKatherine M Szigety, Terrence B Crowley, Kimberly B Gaiser, et al.
Database : the Journal of Biological Databases and Curation|September 25, 2025
Automatic genetic phenotype normalization from dysmorphology physical examinations: an overview of the BioCreative VIII-Task 3 competitionDavy Weissenbacher, Xinwei Zhao, Jessica R C Priestley, et al.
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Showing results (81-90 of 86) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 86 results.
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2014
Mutation of Plekha7 attenuates salt-sensitive hypertension in the ratBradley T Endres, Jessica R C Priestley, Oleg Palygin, et al.
International Journal of Neonatal Screening|April 25, 2022
Newborn Screening for X-Linked Adrenoleukodystrophy: Review of Data and Outcomes in PennsylvaniaJessica R C Priestley, Laura A Adang, Sarah Drewes Williams, et al.
Molecular Genetics and Metabolism Reports|November 24, 2022
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signatureJessica R C Priestley, Lisa M Pace, Kuntal Sen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 1, 2023
Monoallelic loss-of-function BMP2 variants result in BMP2-related skeletal dysplasia spectrumJessica R C Priestley, Ashish R Deshwar, Harsha Murthy, et al.
Pediatrics|June 1, 2022
Clinical Effectiveness of Telemedicine-Based Pediatric Genetics CareKatherine M Szigety, Terrence B Crowley, Kimberly B Gaiser, et al.
Database : the Journal of Biological Databases and Curation|September 25, 2025
Automatic genetic phenotype normalization from dysmorphology physical examinations: an overview of the BioCreative VIII-Task 3 competitionDavy Weissenbacher, Xinwei Zhao, Jessica R C Priestley, et al.
Pageof 9