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Elaine Fletcher

Showing results (1-10 of 9) with videos related to

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Wellcome Open Research|June 10, 2020
Sodium channel myotonia may be associated with high-risk brief resolved unexplained eventsGabriel Cea, Daniel Andreu, Elaine Fletcher, et al.
Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft|December 18, 2016
Oxygen flux reduces Cux1 positive neurons and cortical growth in a gestational rodent model of growth restrictionElaine Fletcher, Jean Wade, Petrina A Georgala, et al.
Lancet (London, England)|June 14, 2014
Indicators linking health and sustainability in the post-2015 development agendaCarlos Dora, Andy Haines, John Balbus, et al.
Neuromuscular Disorders : NMD|March 29, 2025
Late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition: a case series from the West of ScotlandTaylor Watson-Fargie, Autumn Coomber, Rachel Edwards, et al.
Journal of Bone and Mineral Metabolism|December 14, 2017
Genetic analysis of adults heterozygous for ALPL mutationsAgnès Taillandier, Christelle Domingues, Annika Dufour, et al.
Molecular Genetics and Metabolism|September 17, 2013
Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxaAikaterini Dimopoulou, Björn Fischer, Thatjana Gardeitchik, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotypeEmma M Wade, Zandra A Jenkins, Philip B Daniel, et al.
American Journal of Human Genetics|July 19, 2016
Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal DysplasiaEmma M Wade, Philip B Daniel, Zandra A Jenkins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2026
RNU4ATAC-opathy: Clinical, molecular and transcriptomic insights from a large cohortDena R Matalon, Angela L Duker, Taylor M Arriaga, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Wellcome Open Research|June 10, 2020
Sodium channel myotonia may be associated with high-risk brief resolved unexplained eventsGabriel Cea, Daniel Andreu, Elaine Fletcher, et al.
Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft|December 18, 2016
Oxygen flux reduces Cux1 positive neurons and cortical growth in a gestational rodent model of growth restrictionElaine Fletcher, Jean Wade, Petrina A Georgala, et al.
Lancet (London, England)|June 14, 2014
Indicators linking health and sustainability in the post-2015 development agendaCarlos Dora, Andy Haines, John Balbus, et al.
Neuromuscular Disorders : NMD|March 29, 2025
Late-onset multiple-acyl-CoA-dehydrogenase deficiency-like condition: a case series from the West of ScotlandTaylor Watson-Fargie, Autumn Coomber, Rachel Edwards, et al.
Journal of Bone and Mineral Metabolism|December 14, 2017
Genetic analysis of adults heterozygous for ALPL mutationsAgnès Taillandier, Christelle Domingues, Annika Dufour, et al.
Molecular Genetics and Metabolism|September 17, 2013
Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxaAikaterini Dimopoulou, Björn Fischer, Thatjana Gardeitchik, et al.
American Journal of Medical Genetics. Part A|May 13, 2017
Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotypeEmma M Wade, Zandra A Jenkins, Philip B Daniel, et al.
American Journal of Human Genetics|July 19, 2016
Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal DysplasiaEmma M Wade, Philip B Daniel, Zandra A Jenkins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2026
RNU4ATAC-opathy: Clinical, molecular and transcriptomic insights from a large cohortDena R Matalon, Angela L Duker, Taylor M Arriaga, et al.
Pageof 1