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Hane Lee

Showing results (1-10 of 134) with videos related to

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Current Opinion in Genetics & Development|June 30, 2020
The frontiers of sequencing in undiagnosed neurodevelopmental diseasesHane Lee, Stanley F Nelson
Molecular Genetics & Genomic Medicine|October 25, 2023
A novel de novo frameshift variant in the CHD2 gene related to intellectual and developmental disability, seizures and speech problemsAtefeh Mir, Yongjun Song, Hane Lee, et al.
Annals of Human Genetics|August 17, 2023
A novel heterozygous truncating variant in the AGO1 gene in an Iranian family with schizophrenia as an unreported symptomAtefeh Mir, Erfan Khorram, Yongjun Song, et al.
The Journal of Biological Chemistry|November 19, 2002
Characterization of the movement of the kinesin motor KIF1A in living cultured neuronsJae-Ran Lee, Hyewon Shin, Jaewon Ko, et al.
Laboratory Medicine|July 19, 2023
Molecular and phenotypical findings of a novel de novo SYNGAP1 gene variant in an 11-year-old Iranian boy with intellectual disabilityAtefeh Mir, Yongjun Song, Hane Lee, et al.
Annals of the New York Academy of Sciences|August 8, 2015
Clinical exome sequencing in neurogenetic and neuropsychiatric disordersBrent L Fogel, Hane Lee, Samuel P Strom, et al.
The Lancet. Neurology|April 15, 2019
Clinical application of next-generation sequencing to the practice of neurologyJessica Rexach, Hane Lee, Julian A Martinez-Agosto, et al.
Molecular Genetics & Genomic Medicine|July 27, 2023
A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature reviewAtefeh Mir, Yongjun Song, Hane Lee, et al.
Headache|December 18, 2007
Phenotypic and genetic analysis of a large family with migraine-associated vertigoHane Lee, Joanna C Jen, Yoon-Hee Cha, et al.
Archives of Neurology|May 16, 2007
A new episodic ataxia syndrome with linkage to chromosome 19q13Kevin A Kerber, Joanna C Jen, Hane Lee, et al.
Pageof 14

Showing results (1-10 of 134) with videos related to

Sort By:
Pageof 14
Current Opinion in Genetics & Development|June 30, 2020
The frontiers of sequencing in undiagnosed neurodevelopmental diseasesHane Lee, Stanley F Nelson
Molecular Genetics & Genomic Medicine|October 25, 2023
A novel de novo frameshift variant in the CHD2 gene related to intellectual and developmental disability, seizures and speech problemsAtefeh Mir, Yongjun Song, Hane Lee, et al.
Annals of Human Genetics|August 17, 2023
A novel heterozygous truncating variant in the AGO1 gene in an Iranian family with schizophrenia as an unreported symptomAtefeh Mir, Erfan Khorram, Yongjun Song, et al.
The Journal of Biological Chemistry|November 19, 2002
Characterization of the movement of the kinesin motor KIF1A in living cultured neuronsJae-Ran Lee, Hyewon Shin, Jaewon Ko, et al.
Laboratory Medicine|July 19, 2023
Molecular and phenotypical findings of a novel de novo SYNGAP1 gene variant in an 11-year-old Iranian boy with intellectual disabilityAtefeh Mir, Yongjun Song, Hane Lee, et al.
Annals of the New York Academy of Sciences|August 8, 2015
Clinical exome sequencing in neurogenetic and neuropsychiatric disordersBrent L Fogel, Hane Lee, Samuel P Strom, et al.
The Lancet. Neurology|April 15, 2019
Clinical application of next-generation sequencing to the practice of neurologyJessica Rexach, Hane Lee, Julian A Martinez-Agosto, et al.
Molecular Genetics & Genomic Medicine|July 27, 2023
A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature reviewAtefeh Mir, Yongjun Song, Hane Lee, et al.
Headache|December 18, 2007
Phenotypic and genetic analysis of a large family with migraine-associated vertigoHane Lee, Joanna C Jen, Yoon-Hee Cha, et al.
Archives of Neurology|May 16, 2007
A new episodic ataxia syndrome with linkage to chromosome 19q13Kevin A Kerber, Joanna C Jen, Hane Lee, et al.
Pageof 14