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Jennifer C Dempsey

Showing results (21-30 of 44) with videos related to

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Diabetes Research and Clinical Practice|November 10, 2004
A case-control study of maternal recreational physical activity and risk of gestational diabetes mellitusJennifer C Dempsey, Carole L Butler, Tanya K Sorensen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 10, 2013
Persistent figure-eight and side-to-side head shaking is a marker for rhombencephalosynapsisHannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Human Mutation|June 23, 2015
KIAA0586 is Mutated in Joubert SyndromeRuxandra Bachmann-Gagescu, Ian G Phelps, Jennifer C Dempsey, et al.
Brain : a Journal of Neurology|March 28, 2012
Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severityGisele E Ishak, Jennifer C Dempsey, Dennis W W Shaw, et al.
Plos One|January 21, 2026
The impact of delayed evacuation on the quality of human fetal tissueYasmeen Otaibi, Kevin Lee, Lucinda Cort, et al.
Human Molecular Genetics|July 2, 2015
Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genesRenske Oegema, Thomas D Cushion, Ian G Phelps, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Beyond Gómez-López-Hernández syndrome: recurring phenotypic themes in rhombencephalosynapsisHannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Stem Cell Reports|June 23, 2023
Donor perspectives on informed consent and use of biospecimens for brain organoid researchKatherine E MacDuffie, Jason L Stein, Dan Doherty, et al.
Journal of Medical Genetics|January 14, 2012
Genotype-phenotype correlation in CC2D2A-related Joubert syndrome reveals an association with ventriculomegaly and seizuresRuxandra Bachmann-Gagescu, Gisele E Ishak, Jennifer C Dempsey, et al.
American Journal of Human Genetics|April 5, 2016
Recessive Inactivating Mutations in TBCK, Encoding a Rab GTPase-Activating Protein, Cause Severe Infantile Syndromic EncephalopathyJessica X Chong, Viviana Caputo, Ian G Phelps, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Diabetes Research and Clinical Practice|November 10, 2004
A case-control study of maternal recreational physical activity and risk of gestational diabetes mellitusJennifer C Dempsey, Carole L Butler, Tanya K Sorensen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 10, 2013
Persistent figure-eight and side-to-side head shaking is a marker for rhombencephalosynapsisHannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Human Mutation|June 23, 2015
KIAA0586 is Mutated in Joubert SyndromeRuxandra Bachmann-Gagescu, Ian G Phelps, Jennifer C Dempsey, et al.
Brain : a Journal of Neurology|March 28, 2012
Rhombencephalosynapsis: a hindbrain malformation associated with incomplete separation of midbrain and forebrain, hydrocephalus and a broad spectrum of severityGisele E Ishak, Jennifer C Dempsey, Dennis W W Shaw, et al.
Plos One|January 21, 2026
The impact of delayed evacuation on the quality of human fetal tissueYasmeen Otaibi, Kevin Lee, Lucinda Cort, et al.
Human Molecular Genetics|July 2, 2015
Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genesRenske Oegema, Thomas D Cushion, Ian G Phelps, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Beyond Gómez-López-Hernández syndrome: recurring phenotypic themes in rhombencephalosynapsisHannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Stem Cell Reports|June 23, 2023
Donor perspectives on informed consent and use of biospecimens for brain organoid researchKatherine E MacDuffie, Jason L Stein, Dan Doherty, et al.
Journal of Medical Genetics|January 14, 2012
Genotype-phenotype correlation in CC2D2A-related Joubert syndrome reveals an association with ventriculomegaly and seizuresRuxandra Bachmann-Gagescu, Gisele E Ishak, Jennifer C Dempsey, et al.
American Journal of Human Genetics|April 5, 2016
Recessive Inactivating Mutations in TBCK, Encoding a Rab GTPase-Activating Protein, Cause Severe Infantile Syndromic EncephalopathyJessica X Chong, Viviana Caputo, Ian G Phelps, et al.
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