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Showing results (31-40 of 36) with videos related to

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Clinical Pharmacology and Therapeutics|May 6, 2011
Effects of valproic acid on organic acid metabolism in children: a metabolic profiling studyK E Price, R E Pearce, U C Garg, et al.
Genetics in Medicine Open|December 13, 2024
Prospective characterization of early symptom onset and progression in young pediatric patients with variants in the <i>G</i> <i>LA</i> gene across 5 years: Longitudinal data from the Fabry MOPPet StudyD A Laney, M F Houde, A L Foley, et al.
Molecular Genetics and Metabolism|November 28, 2006
Expanded newborn screening identifies maternal primary carnitine deficiencyLisa A Schimmenti, Eric A Crombez, Bernd C Schwahn, et al.
Science Translational Medicine|December 5, 2014
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disordersSarah E Soden, Carol J Saunders, Laurel K Willig, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 31, 2023
Insurance denials and diagnostic rates in a pediatric genomic research cohortTricia N Zion, Courtney D Berrios, Ana S A Cohen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2022
Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomesAna S A Cohen, Emily G Farrow, Ahmed T Abdelmoity, et al.
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Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Clinical Pharmacology and Therapeutics|May 6, 2011
Effects of valproic acid on organic acid metabolism in children: a metabolic profiling studyK E Price, R E Pearce, U C Garg, et al.
Genetics in Medicine Open|December 13, 2024
Prospective characterization of early symptom onset and progression in young pediatric patients with variants in the <i>G</i> <i>LA</i> gene across 5 years: Longitudinal data from the Fabry MOPPet StudyD A Laney, M F Houde, A L Foley, et al.
Molecular Genetics and Metabolism|November 28, 2006
Expanded newborn screening identifies maternal primary carnitine deficiencyLisa A Schimmenti, Eric A Crombez, Bernd C Schwahn, et al.
Science Translational Medicine|December 5, 2014
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disordersSarah E Soden, Carol J Saunders, Laurel K Willig, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 31, 2023
Insurance denials and diagnostic rates in a pediatric genomic research cohortTricia N Zion, Courtney D Berrios, Ana S A Cohen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2022
Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomesAna S A Cohen, Emily G Farrow, Ahmed T Abdelmoity, et al.
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