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David Francis

Showing results (161-170 of 176) with videos related to

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Frontiers in Psychology|February 21, 2022
Shorebirds' Longer Migratory Distances Are Associated With Larger <i>ADCYAP1</i> Microsatellites and Greater Morphological Complexity of Hippocampal AstrocytesDiego de Almeida Miranda, Juliana Araripe, Nara G de Morais Magalhães, et al.
The European Journal of Neuroscience|May 15, 2020
Contrasting migratory journeys and changes in hippocampal astrocyte morphology in shorebirdsEdiely Pereira Henrique, Marcus Augusto de Oliveira, Dario Carvalho Paulo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 testsAlison Dalton Archibald, Melanie Jane Smith, Trent Burgess, et al.
Molecular Autism|May 11, 2019
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic featuresEmma K Baker, Marta Arpone, Solange M Aliaga, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 testsAlison Dalton Archibald, Melanie Jane Smith, Trent Burgess, et al.
The American Journal of Gastroenterology|April 8, 2025
The San Diego Consensus for Laryngopharyngeal Symptoms and Laryngopharyngeal Reflux DiseaseRena Yadlapati, Philip Weissbrod, Erin Walsh, et al.
Genome Research|May 10, 2013
NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traitsPiotr Dittwald, Tomasz Gambin, Przemyslaw Szafranski, et al.
Journal of Medical Genetics|November 6, 2021
Lessons learnt from multifaceted diagnostic approaches to the first 150 families in Victoria's Undiagnosed Diseases ProgramThomas Cloney, Lyndon Gallacher, Lynn S Pais, et al.
American Journal of Human Genetics|August 30, 2016
DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human GenomeRicky S Joshi, Paras Garg, Noah Zaitlen, et al.
Nature Genetics|September 19, 2018
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylationM Felicia Basilicata, Ange-Line Bruel, Giuseppe Semplicio, et al.
Pageof 18

Showing results (161-170 of 176) with videos related to

Sort By:
Pageof 18
Frontiers in Psychology|February 21, 2022
Shorebirds' Longer Migratory Distances Are Associated With Larger <i>ADCYAP1</i> Microsatellites and Greater Morphological Complexity of Hippocampal AstrocytesDiego de Almeida Miranda, Juliana Araripe, Nara G de Morais Magalhães, et al.
The European Journal of Neuroscience|May 15, 2020
Contrasting migratory journeys and changes in hippocampal astrocyte morphology in shorebirdsEdiely Pereira Henrique, Marcus Augusto de Oliveira, Dario Carvalho Paulo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2018
Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 testsAlison Dalton Archibald, Melanie Jane Smith, Trent Burgess, et al.
Molecular Autism|May 11, 2019
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic featuresEmma K Baker, Marta Arpone, Solange M Aliaga, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 testsAlison Dalton Archibald, Melanie Jane Smith, Trent Burgess, et al.
The American Journal of Gastroenterology|April 8, 2025
The San Diego Consensus for Laryngopharyngeal Symptoms and Laryngopharyngeal Reflux DiseaseRena Yadlapati, Philip Weissbrod, Erin Walsh, et al.
Genome Research|May 10, 2013
NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traitsPiotr Dittwald, Tomasz Gambin, Przemyslaw Szafranski, et al.
Journal of Medical Genetics|November 6, 2021
Lessons learnt from multifaceted diagnostic approaches to the first 150 families in Victoria's Undiagnosed Diseases ProgramThomas Cloney, Lyndon Gallacher, Lynn S Pais, et al.
American Journal of Human Genetics|August 30, 2016
DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human GenomeRicky S Joshi, Paras Garg, Noah Zaitlen, et al.
Nature Genetics|September 19, 2018
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylationM Felicia Basilicata, Ange-Line Bruel, Giuseppe Semplicio, et al.
Pageof 18