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Tugce B Balci

Showing results (11-20 of 35) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 21, 2017
Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndromeTugce B Balci, Jorge Davila, Denice Lewis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2020
Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classesWillie H Chang, Pouria Mashouri, Alexander X Lozano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2020
Correction: Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classesWillie H Chang, Pouria Mashouri, Alexander X Lozano, et al.
Plos One|November 24, 2011
A unique role of GATA1s in Down syndrome acute megakaryocytic leukemia biology and therapyAna C Xavier, Holly Edwards, Alan A Dombkowski, et al.
American Journal of Medical Genetics. Part A|January 22, 2020
Tatton-Brown-Rahman syndrome: Six individuals with novel featuresTugce B Balci, Alana Strong, Jennifer M Kalish, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|April 13, 2025
Clinical Implementation and Outcomes of Genetic Testing for Epilepsy by the Ontario Epilepsy Genetic Testing ProgramTugce B Balci, Laila C Schenkel, Cassandra Rastin, et al.
The Journal of Clinical Investigation|May 5, 2015
BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterationsAnindita Basak, Miroslava Hancarova, Jacob C Ulirsch, et al.
American Journal of Medical Genetics. Part A|May 31, 2021
Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variantsCaitlin A Chang, Renee Perrier, Kyle C Kurek, et al.
Clinical Genetics|June 23, 2025
Diagnostic Utility of Exome Data Reanalysis After In Silico Multi-Gene Panels or Clinical Exome Testing for Patients With Epilepsy and Developmental Delay/Intellectual Disability: A Retrospective Cohort StudyAlexanne Cuillerier, Andrea Goodman, Chloe Lawrence, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2021
Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disordersBekim Sadikovic, Michael A Levy, Jennifer Kerkhof, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 21, 2017
Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndromeTugce B Balci, Jorge Davila, Denice Lewis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2020
Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classesWillie H Chang, Pouria Mashouri, Alexander X Lozano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2020
Correction: Phenotate: crowdsourcing phenotype annotations as exercises in undergraduate classesWillie H Chang, Pouria Mashouri, Alexander X Lozano, et al.
Plos One|November 24, 2011
A unique role of GATA1s in Down syndrome acute megakaryocytic leukemia biology and therapyAna C Xavier, Holly Edwards, Alan A Dombkowski, et al.
American Journal of Medical Genetics. Part A|January 22, 2020
Tatton-Brown-Rahman syndrome: Six individuals with novel featuresTugce B Balci, Alana Strong, Jennifer M Kalish, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|April 13, 2025
Clinical Implementation and Outcomes of Genetic Testing for Epilepsy by the Ontario Epilepsy Genetic Testing ProgramTugce B Balci, Laila C Schenkel, Cassandra Rastin, et al.
The Journal of Clinical Investigation|May 5, 2015
BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterationsAnindita Basak, Miroslava Hancarova, Jacob C Ulirsch, et al.
American Journal of Medical Genetics. Part A|May 31, 2021
Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variantsCaitlin A Chang, Renee Perrier, Kyle C Kurek, et al.
Clinical Genetics|June 23, 2025
Diagnostic Utility of Exome Data Reanalysis After In Silico Multi-Gene Panels or Clinical Exome Testing for Patients With Epilepsy and Developmental Delay/Intellectual Disability: A Retrospective Cohort StudyAlexanne Cuillerier, Andrea Goodman, Chloe Lawrence, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2021
Correction: Clinical epigenomics: genome-wide DNA methylation analysis for the diagnosis of Mendelian disordersBekim Sadikovic, Michael A Levy, Jennifer Kerkhof, et al.
Pageof 4