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Abidemi Adegbola

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American Journal of Medical Genetics. Part A|January 19, 2008
A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD)Abidemi Adegbola, Hanlin Gao, Steve Sommer, et al.
Stem Cells Translational Medicine|October 14, 2017
Concise Review: Induced Pluripotent Stem Cell Models for Neuropsychiatric DiseasesAbidemi Adegbola, Luke A Bury, Chen Fu, et al.
HGG Advances|March 15, 2021
Disruption of <i>CTNND2</i>, encoding delta-catenin, causes a penetrant attention deficit disorder and myopiaAbidemi Adegbola, Richard Lutz, Elina Nikkola, et al.
HGG Advances|September 16, 2021
<i>PTPN4</i> germline variants result in aberrant neurodevelopment and growthJoanna J Chmielewska, Deepika Burkardt, Jorge Luis Granadillo, et al.
European Journal of Human Genetics : EJHG|March 12, 2015
Redefining the MED13L syndromeAbidemi Adegbola, Luciana Musante, Bert Callewaert, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|January 19, 2008
A novel mutation in JARID1C/SMCX in a patient with autism spectrum disorder (ASD)Abidemi Adegbola, Hanlin Gao, Steve Sommer, et al.
Stem Cells Translational Medicine|October 14, 2017
Concise Review: Induced Pluripotent Stem Cell Models for Neuropsychiatric DiseasesAbidemi Adegbola, Luke A Bury, Chen Fu, et al.
HGG Advances|March 15, 2021
Disruption of <i>CTNND2</i>, encoding delta-catenin, causes a penetrant attention deficit disorder and myopiaAbidemi Adegbola, Richard Lutz, Elina Nikkola, et al.
HGG Advances|September 16, 2021
<i>PTPN4</i> germline variants result in aberrant neurodevelopment and growthJoanna J Chmielewska, Deepika Burkardt, Jorge Luis Granadillo, et al.
European Journal of Human Genetics : EJHG|March 12, 2015
Redefining the MED13L syndromeAbidemi Adegbola, Luciana Musante, Bert Callewaert, et al.
Pageof 1