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Scott C Smith

Showing results (11-20 of 24) with videos related to

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Molecular Neurobiology|December 16, 2016
Proapoptotic Requirement of Ribosomal Protein L11 in Ribosomal Stress-Challenged Cortical NeuronsLukasz P Slomnicki, Justin Hallgren, Aruna Vashishta, et al.
Leukemia Research|June 15, 2020
MECOM rearrangement involving the MYC locus: Two additional patients with the rare translocation, t(3;8)(q26.2;q24), and molecular reviewScott C Smith, Tareq Z S Qdaisat, Pamela A Althof, et al.
American Journal of Medical Genetics. Part A|July 25, 2020
The recurrent TUBB3 Gly98Ser substitution is the first described to inconsistently result in CFEOM3Scott C Smith, Ann Haskins Olney, Angela Beavers, et al.
American Journal of Medical Genetics. Part A|March 20, 2025
Proximal Deletions of 14q32.2 Result in Severe Neurodevelopmental Outcomes, Congenital Anomalies, and Dysmorphic FeaturesJennifer Black, Robert Roger Lebel, Ria Garg, et al.
Molecular Neurobiology|March 17, 2018
RNA Polymerase 1 Is Transiently Regulated by Seizures and Plays a Role in a Pharmacological Kindling Model of EpilepsyAruna Vashishta, Lukasz P Slomnicki, Maciej Pietrzak, et al.
The Journal of Molecular Diagnostics : JMD|October 20, 2020
Clinical Validation of Somatic Mutation Detection by the OncoScan CNV Plus AssayScott C Smith, Midhat S Farooqi, Melissa A Gener, et al.
Translational Behavioral Medicine|February 1, 2018
Interprofessional case conference: impact on learner outcomesJeffrey Sordahl, India C King, Kyle Davis, et al.
Journal of Medical Genetics|January 16, 2026
Clinical manifestations of chromosome 19p13.11 duplicationDibyendu Dutta, Megan Keeney, Nicole Matthews, et al.
Human Mutation|December 28, 2021
Functionally impaired RPL8 variants associated with Diamond-Blackfan anemia and a Diamond-Blackfan anemia-like phenotypeSimon Lebaron, Marie-Françoise O'Donohue, Scott C Smith, et al.
The Journal of Molecular Diagnostics : JMD|February 6, 2022
Development and Validation of Two RT-qPCR Diagnostic Assays for Detecting Severe Acute Respiratory Syndrome Coronavirus 2 Genomic Targets across Two Specimen TypesEric W Miller, Celeste M Lamberson, Ratilal R Akabari, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Molecular Neurobiology|December 16, 2016
Proapoptotic Requirement of Ribosomal Protein L11 in Ribosomal Stress-Challenged Cortical NeuronsLukasz P Slomnicki, Justin Hallgren, Aruna Vashishta, et al.
Leukemia Research|June 15, 2020
MECOM rearrangement involving the MYC locus: Two additional patients with the rare translocation, t(3;8)(q26.2;q24), and molecular reviewScott C Smith, Tareq Z S Qdaisat, Pamela A Althof, et al.
American Journal of Medical Genetics. Part A|July 25, 2020
The recurrent TUBB3 Gly98Ser substitution is the first described to inconsistently result in CFEOM3Scott C Smith, Ann Haskins Olney, Angela Beavers, et al.
American Journal of Medical Genetics. Part A|March 20, 2025
Proximal Deletions of 14q32.2 Result in Severe Neurodevelopmental Outcomes, Congenital Anomalies, and Dysmorphic FeaturesJennifer Black, Robert Roger Lebel, Ria Garg, et al.
Molecular Neurobiology|March 17, 2018
RNA Polymerase 1 Is Transiently Regulated by Seizures and Plays a Role in a Pharmacological Kindling Model of EpilepsyAruna Vashishta, Lukasz P Slomnicki, Maciej Pietrzak, et al.
The Journal of Molecular Diagnostics : JMD|October 20, 2020
Clinical Validation of Somatic Mutation Detection by the OncoScan CNV Plus AssayScott C Smith, Midhat S Farooqi, Melissa A Gener, et al.
Translational Behavioral Medicine|February 1, 2018
Interprofessional case conference: impact on learner outcomesJeffrey Sordahl, India C King, Kyle Davis, et al.
Journal of Medical Genetics|January 16, 2026
Clinical manifestations of chromosome 19p13.11 duplicationDibyendu Dutta, Megan Keeney, Nicole Matthews, et al.
Human Mutation|December 28, 2021
Functionally impaired RPL8 variants associated with Diamond-Blackfan anemia and a Diamond-Blackfan anemia-like phenotypeSimon Lebaron, Marie-Françoise O'Donohue, Scott C Smith, et al.
The Journal of Molecular Diagnostics : JMD|February 6, 2022
Development and Validation of Two RT-qPCR Diagnostic Assays for Detecting Severe Acute Respiratory Syndrome Coronavirus 2 Genomic Targets across Two Specimen TypesEric W Miller, Celeste M Lamberson, Ratilal R Akabari, et al.
Pageof 3