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Samin A Sajan

Showing results (1-10 of 19) with videos related to

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Annual Review of Genomics and Human Genetics|June 19, 2012
Methods for identifying higher-order chromatin structureSamin A Sajan, R David Hawkins
Genetics|July 31, 2007
Toward a systems biology of mouse inner ear organogenesis: gene expression pathways, patterns and network analysisSamin A Sajan, Mark E Warchol, Michael Lovett
Cerebellum (London, England)|April 14, 2010
Novel approaches to studying the genetic basis of cerebellar developmentSamin A Sajan, Kathryn E Waimey, Kathleen J Millen
Human Molecular Genetics|January 14, 2011
Identification of direct downstream targets of Dlx5 during early inner ear developmentSamin A Sajan, John L R Rubenstein, Mark E Warchol, et al.
Clinical Case Reports|July 11, 2018
Diagnostic exome sequencing identifies <i>GLI2</i> haploinsufficiency and chromosome 20 uniparental disomy in a patient with developmental anomaliesSamin A Sajan, Zöe Powis, Katherine L Helbig, et al.
Journal of Medical Genetics|November 28, 2018
Biallelic disruption of <i>PKDCC</i> is associated with a skeletal disorder characterised by rhizomelic shortening of extremities and dysmorphic featuresSamin A Sajan, Jaya Ganesh, Deepali N Shinde, et al.
Plos One|June 15, 2007
Large scale gene expression profiles of regenerating inner ear sensory epitheliaR David Hawkins, Stavros Bashiardes, Kara E Powder, et al.
Clinical Genetics|October 20, 2019
Clinical diagnostic exome sequencing in dystonia: Genetic testing challenges for complex conditionsZöe Powis, Meghan C Towne, Kelly D F Hagman, et al.
American Journal of Medical Genetics. Part A|August 8, 2023
The smallest likely pathogenic duplication of a SOX9 enhancer identified to date in a family with 46,XX testicular differences of sex developmentSamin A Sajan, Carolyn M Brown, Laura Davis-Keppen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2019
A retrospective review of multiple findings in diagnostic exome sequencing: half are distinct and half are overlapping diagnosesErica D Smith, Kirsten Blanco, Samin A Sajan, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Annual Review of Genomics and Human Genetics|June 19, 2012
Methods for identifying higher-order chromatin structureSamin A Sajan, R David Hawkins
Genetics|July 31, 2007
Toward a systems biology of mouse inner ear organogenesis: gene expression pathways, patterns and network analysisSamin A Sajan, Mark E Warchol, Michael Lovett
Cerebellum (London, England)|April 14, 2010
Novel approaches to studying the genetic basis of cerebellar developmentSamin A Sajan, Kathryn E Waimey, Kathleen J Millen
Human Molecular Genetics|January 14, 2011
Identification of direct downstream targets of Dlx5 during early inner ear developmentSamin A Sajan, John L R Rubenstein, Mark E Warchol, et al.
Clinical Case Reports|July 11, 2018
Diagnostic exome sequencing identifies <i>GLI2</i> haploinsufficiency and chromosome 20 uniparental disomy in a patient with developmental anomaliesSamin A Sajan, Zöe Powis, Katherine L Helbig, et al.
Journal of Medical Genetics|November 28, 2018
Biallelic disruption of <i>PKDCC</i> is associated with a skeletal disorder characterised by rhizomelic shortening of extremities and dysmorphic featuresSamin A Sajan, Jaya Ganesh, Deepali N Shinde, et al.
Plos One|June 15, 2007
Large scale gene expression profiles of regenerating inner ear sensory epitheliaR David Hawkins, Stavros Bashiardes, Kara E Powder, et al.
Clinical Genetics|October 20, 2019
Clinical diagnostic exome sequencing in dystonia: Genetic testing challenges for complex conditionsZöe Powis, Meghan C Towne, Kelly D F Hagman, et al.
American Journal of Medical Genetics. Part A|August 8, 2023
The smallest likely pathogenic duplication of a SOX9 enhancer identified to date in a family with 46,XX testicular differences of sex developmentSamin A Sajan, Carolyn M Brown, Laura Davis-Keppen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2019
A retrospective review of multiple findings in diagnostic exome sequencing: half are distinct and half are overlapping diagnosesErica D Smith, Kirsten Blanco, Samin A Sajan, et al.
Pageof 2