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Showing results (291-300 of 344) with videos related to

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Epilepsy Research|February 16, 2017
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsyPiero Perucca, Ingrid E Scheffer, A Simon Harvey, et al.
BMJ Paediatrics Open|April 12, 2018
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohortLilian Downie, Jane L Halliday, Rachel A Burt, et al.
Zootaxa|July 6, 2026
<b>Description of all stages of a new tick species from California, <i>Haemaphysalis vespertina</i> (Acari: Ixodidae), with redescription of <i>H. leporispalustris</i> Packard, 1869 adults and phylogenetic relationships among related U.S. taxa</b>Andrea Egizi, Santiago Nava, Angie Nakano, et al.
Vector Borne and Zoonotic Diseases (Larchmont, N.Y.)|April 4, 2019
Multistate Survey of American Dog Ticks (<i>Dermacentor variabilis</i>) for <i>Rickettsia</i> SpeciesJoy A Hecht, Michelle E J Allerdice, Elizabeth A Dykstra, et al.
Nutrients|August 26, 2023
Evaluation of a New Glycomacropeptide-Based Protein Substitute in Powdered and Liquid Format in Patients with PKUMarta Delsoglio, Rebecca Capener, Anita MacDonald, et al.
European Journal of Human Genetics : EJHG|December 13, 2019
Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Nutrients|August 26, 2023
Evaluation of a New 'Mix-In' Style Glycomacropeptide-Based Protein Substitute for Food and Drinks in Patients with Phenylketonuria and TyrosinemiaMarta Delsoglio, Rebecca Capener, Anita MacDonald, et al.
Molecular Ecology Resources|March 19, 2016
Simultaneous identification of host, ectoparasite and pathogen DNA via in-solution captureMichael G Campana, Melissa T R Hawkins, Lauren H Henson, et al.
Genome Medicine|July 29, 2015
Cpipe: a shared variant detection pipeline designed for diagnostic settingsSimon P Sadedin, Harriet Dashnow, Paul A James, et al.
European Journal of Human Genetics : EJHG|November 10, 2020
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Pageof 35

Showing results (291-300 of 344) with videos related to

Sort By:
Pageof 35
Epilepsy Research|February 16, 2017
Real-world utility of whole exome sequencing with targeted gene analysis for focal epilepsyPiero Perucca, Ingrid E Scheffer, A Simon Harvey, et al.
BMJ Paediatrics Open|April 12, 2018
A protocol for whole-exome sequencing in newborns with congenital deafness: a prospective population-based cohortLilian Downie, Jane L Halliday, Rachel A Burt, et al.
Zootaxa|July 6, 2026
<b>Description of all stages of a new tick species from California, <i>Haemaphysalis vespertina</i> (Acari: Ixodidae), with redescription of <i>H. leporispalustris</i> Packard, 1869 adults and phylogenetic relationships among related U.S. taxa</b>Andrea Egizi, Santiago Nava, Angie Nakano, et al.
Vector Borne and Zoonotic Diseases (Larchmont, N.Y.)|April 4, 2019
Multistate Survey of American Dog Ticks (<i>Dermacentor variabilis</i>) for <i>Rickettsia</i> SpeciesJoy A Hecht, Michelle E J Allerdice, Elizabeth A Dykstra, et al.
Nutrients|August 26, 2023
Evaluation of a New Glycomacropeptide-Based Protein Substitute in Powdered and Liquid Format in Patients with PKUMarta Delsoglio, Rebecca Capener, Anita MacDonald, et al.
European Journal of Human Genetics : EJHG|December 13, 2019
Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Nutrients|August 26, 2023
Evaluation of a New 'Mix-In' Style Glycomacropeptide-Based Protein Substitute for Food and Drinks in Patients with Phenylketonuria and TyrosinemiaMarta Delsoglio, Rebecca Capener, Anita MacDonald, et al.
Molecular Ecology Resources|March 19, 2016
Simultaneous identification of host, ectoparasite and pathogen DNA via in-solution captureMichael G Campana, Melissa T R Hawkins, Lauren H Henson, et al.
Genome Medicine|July 29, 2015
Cpipe: a shared variant detection pipeline designed for diagnostic settingsSimon P Sadedin, Harriet Dashnow, Paul A James, et al.
European Journal of Human Genetics : EJHG|November 10, 2020
Correction: Exome sequencing in infants with congenital hearing impairment: a population-based cohort studyLilian Downie, Jane Halliday, Rachel Burt, et al.
Pageof 35