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David Francis

Showing results (151-160 of 176) with videos related to

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American Journal of Medical Genetics. Part A|November 9, 2022
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndromeEmma K Baker, Marta Arpone, Minh Bui, et al.
Human Molecular Genetics|May 22, 2025
Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variantsNeblina Sikta, Samuel Gooley, Timothy E Green, et al.
Scientific Reports|February 28, 2018
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile XMarta Arpone, Emma K Baker, Lesley Bretherton, et al.
Emerging Microbes & Infections|June 2, 2018
Antigenic characterization of highly pathogenic avian influenza A(H5N1) viruses with chicken and ferret antisera reveals clade-dependent variation in hemagglutination inhibition profilesDiep Thi Nguyen, Samuel S Shepard, David Francis Burke, et al.
International Journal of Molecular Sciences|August 26, 2023
Molecular Changes in the Brain of the Wintering <i>Calidris pusilla</i> in the Mangroves of the Amazon River EstuaryPatrick Douglas Corrêa Pereira, Ediely Pereira Henrique, Emanuel Ramos da Costa, et al.
Australian and New Zealand Journal of Public Health|February 13, 2024
Balancing the risks and benefits of sun exposure: A revised position statement for Australian adultsRachel E Neale, Victoria Beedle, Peter R Ebeling, et al.
Frontiers in Neuroanatomy|November 5, 2019
Differential Change in Hippocampal Radial Astrocytes and Neurogenesis in Shorebirds With Contrasting Migratory RoutesCamila Mendes de Lima, Patrick Douglas Corrêa Pereira, Ediely Pereira Henrique, et al.
JAMA Network Open|January 4, 2022
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic WorkflowDavid E Godler, Ling Ling, Dinusha Gamage, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 13, 2012
Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation studyYoshimi Inaba, Amy S Herlihy, Charles E Schwartz, et al.
Journal of Neurodevelopmental Disorders|December 28, 2019
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndromeEmma K Baker, Marta Arpone, Solange Aliaga Vera, et al.
Pageof 18

Showing results (151-160 of 176) with videos related to

Sort By:
Pageof 18
American Journal of Medical Genetics. Part A|November 9, 2022
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndromeEmma K Baker, Marta Arpone, Minh Bui, et al.
Human Molecular Genetics|May 22, 2025
Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variantsNeblina Sikta, Samuel Gooley, Timothy E Green, et al.
Scientific Reports|February 28, 2018
Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile XMarta Arpone, Emma K Baker, Lesley Bretherton, et al.
Emerging Microbes & Infections|June 2, 2018
Antigenic characterization of highly pathogenic avian influenza A(H5N1) viruses with chicken and ferret antisera reveals clade-dependent variation in hemagglutination inhibition profilesDiep Thi Nguyen, Samuel S Shepard, David Francis Burke, et al.
International Journal of Molecular Sciences|August 26, 2023
Molecular Changes in the Brain of the Wintering <i>Calidris pusilla</i> in the Mangroves of the Amazon River EstuaryPatrick Douglas Corrêa Pereira, Ediely Pereira Henrique, Emanuel Ramos da Costa, et al.
Australian and New Zealand Journal of Public Health|February 13, 2024
Balancing the risks and benefits of sun exposure: A revised position statement for Australian adultsRachel E Neale, Victoria Beedle, Peter R Ebeling, et al.
Frontiers in Neuroanatomy|November 5, 2019
Differential Change in Hippocampal Radial Astrocytes and Neurogenesis in Shorebirds With Contrasting Migratory RoutesCamila Mendes de Lima, Patrick Douglas Corrêa Pereira, Ediely Pereira Henrique, et al.
JAMA Network Open|January 4, 2022
Feasibility of Screening for Chromosome 15 Imprinting Disorders in 16 579 Newborns by Using a Novel Genomic WorkflowDavid E Godler, Ling Ling, Dinusha Gamage, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 13, 2012
Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation studyYoshimi Inaba, Amy S Herlihy, Charles E Schwartz, et al.
Journal of Neurodevelopmental Disorders|December 28, 2019
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndromeEmma K Baker, Marta Arpone, Solange Aliaga Vera, et al.
Pageof 18