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Showing results (561-570 of 915) with videos related to

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Plos Genetics|August 23, 2012
Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathwaysCandice K Silversides, Anath C Lionel, Gregory Costain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorderKate Tsiplova, Richard M Zur, Christian R Marshall, et al.
Schizophrenia Research|July 24, 2007
Molecular analysis of a chromosome 4 inversion segregating in a large schizophrenia kindred from Hong KongAlbert K Mensah, Vincenzo De Luca, Beata Stachowiak, et al.
Journal of Medical Genetics|April 1, 2025
Clinical utility of genome sequencing in autism: illustrative examples from a genomic research studyThanuja Selvanayagam, Ny Hoang, Ege Sarikaya, et al.
The Cochrane Database of Systematic Reviews|May 27, 2025
Yoga for fatigue in people with cancerSarah Messer, Annika Oeser, Carina Wagner, et al.
NPJ Genomic Medicine|January 13, 2025
Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencingDaniele Merico, Nigel Sharfe, Harjit Dadi, et al.
Computational and Structural Biotechnology Journal|January 29, 2024
Combining Off-flow, a Nextflow-coded program, and whole genome sequencing reveals unintended genetic variation in CRISPR/Cas-edited iPSCsCarole Shum, Sang Yeon Han, Bhooma Thiruvahindrapuram, et al.
Human Molecular Genetics|July 4, 2002
Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32Kazuhiko Nakabayashi, Louise Bentley, Megan P Hitchins, et al.
NPJ Genomic Medicine|January 13, 2022
Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delayYi Liu, Yuqiang Lv, Mehdi Zarrei, et al.
Frontiers in Neurology|May 3, 2021
An Epigenetically Distinct Subset of Children With Autism Spectrum Disorder Resulting From Differences in Blood Cell CompositionMaryam Jangjoo, Sarah J Goodman, Sanaa Choufani, et al.
Pageof 92

Showing results (561-570 of 915) with videos related to

Sort By:
Pageof 92
Plos Genetics|August 23, 2012
Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathwaysCandice K Silversides, Anath C Lionel, Gregory Costain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorderKate Tsiplova, Richard M Zur, Christian R Marshall, et al.
Schizophrenia Research|July 24, 2007
Molecular analysis of a chromosome 4 inversion segregating in a large schizophrenia kindred from Hong KongAlbert K Mensah, Vincenzo De Luca, Beata Stachowiak, et al.
Journal of Medical Genetics|April 1, 2025
Clinical utility of genome sequencing in autism: illustrative examples from a genomic research studyThanuja Selvanayagam, Ny Hoang, Ege Sarikaya, et al.
The Cochrane Database of Systematic Reviews|May 27, 2025
Yoga for fatigue in people with cancerSarah Messer, Annika Oeser, Carina Wagner, et al.
NPJ Genomic Medicine|January 13, 2025
Pre-T cell receptor-α immunodeficiency detected exclusively using whole genome sequencingDaniele Merico, Nigel Sharfe, Harjit Dadi, et al.
Computational and Structural Biotechnology Journal|January 29, 2024
Combining Off-flow, a Nextflow-coded program, and whole genome sequencing reveals unintended genetic variation in CRISPR/Cas-edited iPSCsCarole Shum, Sang Yeon Han, Bhooma Thiruvahindrapuram, et al.
Human Molecular Genetics|July 4, 2002
Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32Kazuhiko Nakabayashi, Louise Bentley, Megan P Hitchins, et al.
NPJ Genomic Medicine|January 13, 2022
Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delayYi Liu, Yuqiang Lv, Mehdi Zarrei, et al.
Frontiers in Neurology|May 3, 2021
An Epigenetically Distinct Subset of Children With Autism Spectrum Disorder Resulting From Differences in Blood Cell CompositionMaryam Jangjoo, Sarah J Goodman, Sanaa Choufani, et al.
Pageof 92