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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 mellitus
Jennifer 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 rhombencephalosynapsis
Hannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Human Mutation
|
June 23, 2015
KIAA0586 is Mutated in Joubert Syndrome
Ruxandra 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 severity
Gisele 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 tissue
Yasmeen Otaibi, Kevin Lee, Lucinda Cort, et al.
Human Molecular Genetics
|
July 2, 2015
Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes
Renske 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 rhombencephalosynapsis
Hannah 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 research
Katherine 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 seizures
Ruxandra 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 Encephalopathy
Jessica X Chong, Viviana Caputo, Ian G Phelps, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 44) with videos related to
Sort By:
Page
of 5
Diabetes Research and Clinical Practice
|
November 10, 2004
A case-control study of maternal recreational physical activity and risk of gestational diabetes mellitus
Jennifer 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 rhombencephalosynapsis
Hannah M Tully, Jennifer C Dempsey, Gisele E Ishak, et al.
Human Mutation
|
June 23, 2015
KIAA0586 is Mutated in Joubert Syndrome
Ruxandra 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 severity
Gisele 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 tissue
Yasmeen Otaibi, Kevin Lee, Lucinda Cort, et al.
Human Molecular Genetics
|
July 2, 2015
Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes
Renske 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 rhombencephalosynapsis
Hannah 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 research
Katherine 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 seizures
Ruxandra 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 Encephalopathy
Jessica X Chong, Viviana Caputo, Ian G Phelps, et al.
Page
of 5