Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Flora Tassone

Showing results (11-20 of 348) with videos related to

Pageof 35
Sort By:
Molecular Neurobiology|January 4, 2023
Structure and Alternative Splicing of the Antisense FMR1 (ASFMR1) GeneMarwa Zafarullah, Jie Li, Elizabeth Tseng, et al.
The Journal of Clinical Investigation|December 4, 2012
Fragile X syndrome: causes, diagnosis, mechanisms, and therapeuticsClaudia Bagni, Flora Tassone, Giovanni Neri, et al.
Journal of Neurodevelopmental Disorders|August 30, 2014
Fragile x premutationFlora Tassone, Paul J Hagerman, Randi J Hagerman
Current Genomics|November 2, 2011
Fragile x syndromeYingratana McLennan, Jonathan Polussa, Flora Tassone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 14, 2011
Fragile X-associated tremor ataxia syndrome in FMR1 gray zone allele carriersDeborah Hall, Flora Tassone, Olga Klepitskaya, et al.
Cognitive, Affective & Behavioral Neuroscience|February 28, 2009
Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndromeYukari Takarae, Linda Schmidt, Flora Tassone, et al.
European Journal of Human Genetics : EJHG|May 3, 2012
De novo microduplication of the FMR1 gene in a patient with developmental delay, epilepsy and hyperactivityJaime Vengoechea, Aditi S Parikh, Shulin Zhang, et al.
Journal of Applied Research in Intellectual Disabilities : JARID|July 27, 2016
Down Syndrome and Fragile X Syndrome in a Colombian Woman: Case ReportWilmar Saldarriaga, Fabian Andres Ruiz, Flora Tassone, et al.
Expert Review of Molecular Diagnostics|March 5, 2021
Diagnostic profile of the AmplideX Fragile X Dx and Carrier Screen Kit for diagnosis and screening of fragile X syndrome and other FMR1-related disordersElizabeth Berry-Kravis, Lili Zhou, Jonathan Jackson, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 18, 2020
The emerging molecular mechanisms for mitochondrial dysfunctions in FXTASDhruv Gohel, Nicolas Charlet Berguerand, Flora Tassone, et al.
Pageof 35

Showing results (11-20 of 348) with videos related to

Sort By:
Pageof 35
Molecular Neurobiology|January 4, 2023
Structure and Alternative Splicing of the Antisense FMR1 (ASFMR1) GeneMarwa Zafarullah, Jie Li, Elizabeth Tseng, et al.
The Journal of Clinical Investigation|December 4, 2012
Fragile X syndrome: causes, diagnosis, mechanisms, and therapeuticsClaudia Bagni, Flora Tassone, Giovanni Neri, et al.
Journal of Neurodevelopmental Disorders|August 30, 2014
Fragile x premutationFlora Tassone, Paul J Hagerman, Randi J Hagerman
Current Genomics|November 2, 2011
Fragile x syndromeYingratana McLennan, Jonathan Polussa, Flora Tassone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 14, 2011
Fragile X-associated tremor ataxia syndrome in FMR1 gray zone allele carriersDeborah Hall, Flora Tassone, Olga Klepitskaya, et al.
Cognitive, Affective & Behavioral Neuroscience|February 28, 2009
Catechol-O-methyltransferase polymorphism modulates cognitive control in children with chromosome 22q11.2 deletion syndromeYukari Takarae, Linda Schmidt, Flora Tassone, et al.
European Journal of Human Genetics : EJHG|May 3, 2012
De novo microduplication of the FMR1 gene in a patient with developmental delay, epilepsy and hyperactivityJaime Vengoechea, Aditi S Parikh, Shulin Zhang, et al.
Journal of Applied Research in Intellectual Disabilities : JARID|July 27, 2016
Down Syndrome and Fragile X Syndrome in a Colombian Woman: Case ReportWilmar Saldarriaga, Fabian Andres Ruiz, Flora Tassone, et al.
Expert Review of Molecular Diagnostics|March 5, 2021
Diagnostic profile of the AmplideX Fragile X Dx and Carrier Screen Kit for diagnosis and screening of fragile X syndrome and other FMR1-related disordersElizabeth Berry-Kravis, Lili Zhou, Jonathan Jackson, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 18, 2020
The emerging molecular mechanisms for mitochondrial dysfunctions in FXTASDhruv Gohel, Nicolas Charlet Berguerand, Flora Tassone, et al.
Pageof 35