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Showing results (441-450 of 456) with videos related to

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Nature Communications|October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunctionMichael R Bowl, Michelle M Simon, Neil J Ingham, et al.
Genome Medicine|September 23, 2017
Identification of novel candidate disease genes from de novo exonic copy number variantsTomasz Gambin, Bo Yuan, Weimin Bi, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
JAMA Pediatrics|October 4, 2017
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical ManagementLinyan Meng, Mohan Pammi, Anirudh Saronwala, et al.
American Journal of Human Genetics|February 19, 2019
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia PhenotypesLindsay C Burrage, John J Reynolds, Nissan Vida Baratang, et al.
Nature Genetics|June 27, 2017
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping ConsortiumTerrence F Meehan, Nathalie Conte, David B West, et al.
Nature Communications|January 20, 2018
Identification of genetic elements in metabolism by high-throughput mouse phenotypingJan Rozman, Birgit Rathkolb, Manuela A Oestereicher, et al.
American Journal of Human Genetics|July 2, 2013
TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensitiesWojciech Wiszniewski, Jill V Hunter, Neil A Hanchard, et al.
Communications Biology|December 28, 2018
Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Communications Biology|March 12, 2019
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Pageof 46

Showing results (441-450 of 456) with videos related to

Sort By:
Pageof 46
Nature Communications|October 14, 2017
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunctionMichael R Bowl, Michelle M Simon, Neil J Ingham, et al.
Genome Medicine|September 23, 2017
Identification of novel candidate disease genes from de novo exonic copy number variantsTomasz Gambin, Bo Yuan, Weimin Bi, et al.
Neuron|September 25, 2015
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk LociStephan J Sanders, Xin He, A Jeremy Willsey, et al.
JAMA Pediatrics|October 4, 2017
Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical ManagementLinyan Meng, Mohan Pammi, Anirudh Saronwala, et al.
American Journal of Human Genetics|February 19, 2019
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia PhenotypesLindsay C Burrage, John J Reynolds, Nissan Vida Baratang, et al.
Nature Genetics|June 27, 2017
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping ConsortiumTerrence F Meehan, Nathalie Conte, David B West, et al.
Nature Communications|January 20, 2018
Identification of genetic elements in metabolism by high-throughput mouse phenotypingJan Rozman, Birgit Rathkolb, Manuela A Oestereicher, et al.
American Journal of Human Genetics|July 2, 2013
TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensitiesWojciech Wiszniewski, Jill V Hunter, Neil A Hanchard, et al.
Communications Biology|December 28, 2018
Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Communications Biology|March 12, 2019
Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockoutsBret A Moore, Brian C Leonard, Lionel Sebbag, et al.
Pageof 46