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T Cho

Showing results (301-310 of 375) with videos related to

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Clinical Genetics|December 22, 2017
Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impactJ Wynn, R Ottman, J Duong, et al.
American Journal of Human Genetics|July 8, 2017
REST Final-Exon-Truncating Mutations Cause Hereditary Gingival FibromatosisYavuz Bayram, Janson J White, Nursel Elcioglu, et al.
American Journal of Human Genetics|October 6, 2018
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental SyndromeChristiane K Bauer, Paolo Calligari, Francesca Clementina Radio, et al.
European Journal of Human Genetics : EJHG|February 20, 2019
De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairmentVolkan Okur, Megan T Cho, Richard van Wijk, et al.
Patient Education and Counseling|September 16, 2019
Impact of patient education videos on genetic counseling outcomes after exome sequencingRebecca Hernan, Megan T Cho, Ashley L Wilson, et al.
Physical Review Letters|October 10, 2006
Observation and control of transverse energy-transport barrier due to the formation of an energetic-electron layer with sheared ExB flowT Cho, J Kohagura, T Numakura, et al.
American Journal of Human Genetics|August 25, 2015
Mutations in SPATA5 Are Associated with Microcephaly, Intellectual Disability, Seizures, and Hearing LossAkemi J Tanaka, Megan T Cho, Francisca Millan, et al.
Clinical Genetics|January 24, 2017
Association of the missense variant p.Arg203Trp in PACS1 as a cause of intellectual disability and seizuresD Stern, M T Cho, R Chikarmane, et al.
Biological Psychiatry Global Open Science|July 31, 2023
Illness Phase as a Key Assessment and Intervention Window for PsychosisChristian G Kohler, Daniel H Wolf, Anissa Abi-Dargham, et al.
American Journal of Medical Genetics. Part A|June 24, 2020
Estimating the relative frequency of leukodystrophies and recommendations for carrier screening in the era of next-generation sequencingJohanna L Schmidt, Amy Pizzino, Jessica Nicholl, et al.
Pageof 38

Showing results (301-310 of 375) with videos related to

Sort By:
Pageof 38
Clinical Genetics|December 22, 2017
Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impactJ Wynn, R Ottman, J Duong, et al.
American Journal of Human Genetics|July 8, 2017
REST Final-Exon-Truncating Mutations Cause Hereditary Gingival FibromatosisYavuz Bayram, Janson J White, Nursel Elcioglu, et al.
American Journal of Human Genetics|October 6, 2018
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental SyndromeChristiane K Bauer, Paolo Calligari, Francesca Clementina Radio, et al.
European Journal of Human Genetics : EJHG|February 20, 2019
De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairmentVolkan Okur, Megan T Cho, Richard van Wijk, et al.
Patient Education and Counseling|September 16, 2019
Impact of patient education videos on genetic counseling outcomes after exome sequencingRebecca Hernan, Megan T Cho, Ashley L Wilson, et al.
Physical Review Letters|October 10, 2006
Observation and control of transverse energy-transport barrier due to the formation of an energetic-electron layer with sheared ExB flowT Cho, J Kohagura, T Numakura, et al.
American Journal of Human Genetics|August 25, 2015
Mutations in SPATA5 Are Associated with Microcephaly, Intellectual Disability, Seizures, and Hearing LossAkemi J Tanaka, Megan T Cho, Francisca Millan, et al.
Clinical Genetics|January 24, 2017
Association of the missense variant p.Arg203Trp in PACS1 as a cause of intellectual disability and seizuresD Stern, M T Cho, R Chikarmane, et al.
Biological Psychiatry Global Open Science|July 31, 2023
Illness Phase as a Key Assessment and Intervention Window for PsychosisChristian G Kohler, Daniel H Wolf, Anissa Abi-Dargham, et al.
American Journal of Medical Genetics. Part A|June 24, 2020
Estimating the relative frequency of leukodystrophies and recommendations for carrier screening in the era of next-generation sequencingJohanna L Schmidt, Amy Pizzino, Jessica Nicholl, et al.
Pageof 38