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Human genomics

Showing results (91-100 of 1,249) with videos related to

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Human Genomics|July 3, 2021
Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platformJiexia Yang, Jing Wu, Haishan Peng, et al.
Human Genomics|July 10, 2021
High-throughput screening of circRNAs reveals novel mechanisms of tuberous sclerosis complex-related renal angiomyolipomaYang Zhao, Hao Guo, Wenda Wang, et al.
Human Genomics|June 15, 2021
Correction to: Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparitiesTesfaye B Mersha, Tilahun Abebe
Human Genomics|September 16, 2018
Secondary findings in 421 whole exome-sequenced Chinese childrenWen Chen, Wenke Li, Yi Ma, et al.
Human Genomics|June 30, 2018
Abundance of clinical variants in exons included in multiple transcriptsSankar Subramanian
Human Genomics|September 25, 2016
Variation of global DNA methylation levels with age and in autistic childrenShui-Ying Tsang, Tanveer Ahmad, Flora W K Mat, et al.
Human Genomics|June 24, 2018
The tale of histone modifications and its role in multiple sclerosisHui He, Zhiping Hu, Han Xiao, et al.
Human Genomics|July 6, 2018
A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosaYabin Chen, Li Huang, Xiaodong Jiao, et al.
Human Genomics|June 5, 2019
IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patientsLidiia Zhytnik, Katre Maasalu, Binh Ho Duy, et al.
Human Genomics|January 25, 2021
Correction to: Hyperinsulinism associated with GLUD1 mutation: allosteric regulation and functional characterization of p.G446V glutamate dehydrogenaseKarolina Luczkowska, Caroline Stekelenburg, Frédérique Sloan-Béna, et al.
Pageof 125

Showing results (91-100 of 1,249) with videos related to

Sort By:
Pageof 125
Human Genomics|July 3, 2021
Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platformJiexia Yang, Jing Wu, Haishan Peng, et al.
Human Genomics|July 10, 2021
High-throughput screening of circRNAs reveals novel mechanisms of tuberous sclerosis complex-related renal angiomyolipomaYang Zhao, Hao Guo, Wenda Wang, et al.
Human Genomics|June 15, 2021
Correction to: Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparitiesTesfaye B Mersha, Tilahun Abebe
Human Genomics|September 16, 2018
Secondary findings in 421 whole exome-sequenced Chinese childrenWen Chen, Wenke Li, Yi Ma, et al.
Human Genomics|June 30, 2018
Abundance of clinical variants in exons included in multiple transcriptsSankar Subramanian
Human Genomics|September 25, 2016
Variation of global DNA methylation levels with age and in autistic childrenShui-Ying Tsang, Tanveer Ahmad, Flora W K Mat, et al.
Human Genomics|June 24, 2018
The tale of histone modifications and its role in multiple sclerosisHui He, Zhiping Hu, Han Xiao, et al.
Human Genomics|July 6, 2018
A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosaYabin Chen, Li Huang, Xiaodong Jiao, et al.
Human Genomics|June 5, 2019
IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patientsLidiia Zhytnik, Katre Maasalu, Binh Ho Duy, et al.
Human Genomics|January 25, 2021
Correction to: Hyperinsulinism associated with GLUD1 mutation: allosteric regulation and functional characterization of p.G446V glutamate dehydrogenaseKarolina Luczkowska, Caroline Stekelenburg, Frédérique Sloan-Béna, et al.
Pageof 125