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CHD2
Autism Ontario Genetics Webinar EN.Pdf
De Novo POGZ Mutations in Sporadic
Co-Occupancy by Multiple Cardiac Transcription Factors Identifies
The Landscape of Human Mutually Exclusive Splicing
CHD2 Haploinsufficiency Is Associated with Developmental Delay
Mutations in Frogs Point to Autism Genes' Shared Role in Neurogenesis
CHD2-Related CNS Pathologies
The RNA Splicing Response to DNA Damage
Autism and Cancer Share Risk Genes, Pathways, and Drug Targets
Identification of CHD2 Nuclear Localization Signals
Targeted Resequencing in Epileptic Encephalopathies Identifies De
High-Throughput Single-Cell Functional Elucidation of Neurodevelopmental Disease–Associated Genes Reveals Convergent Mechanisms Altering Neuronal Differentiation
Regulation of CHD2 Expression by the Chaserr Long Noncoding RNA Is Essential for Viability
Chromatin Remodeler CHD8 in Autism and Brain Development
The International Mouse Phenotyping Consortium (IMPC): a Functional
CHD2 Variants Are a Risk Factor for Photosensitivity in Epilepsy
Autismnext Positive Sample Report
Diagnostic Exome Sequencing Provides a Molecular Diagnosis for a Significant Proportion of Patients with Epilepsy
Top View
Prevalence, Phenotype and Architecture of Developmental Disorders Caused by De Novo Mutation
Role of Chromodomain Helicase DNA-Binding Protein 2 in DNA Damage Response Signaling and Tumorigenesis
Massive Sequencing Studies Reveal Key Autism Genes
Impaired Neurodevelopmental Pathways in Autism Spectrum Disorder
Dictyostelium Discoideum James L
Viral-Induced Alternative Splicing of Host Genes Promotes Influenza
Linking Autism Risk Genes to Disruption of Cortical Development
Autism Spectrum Disorder
Isolation and Characterization of the Y32G9A.8 Promoter in C. Elegans
A Novel Genetic Syndrome Caused by Haploinsufficiency of CHD2, a Regulator of Chromatin Structure
Chromatin Landscapes and Genetic Risk in Systemic Lupus Joyce S
SMARCA4 Variants Identified by Targeted Exome-Sequencing of 131,668 Cancer Patients
High-Throughput Single-Cell Functional Elucidation of Neurodevelopmental Disease-Associated Genes Reveals Convergent Mechanisms Altering Neuronal Differentiation
The Emerging Roles of ATP-Dependent Chromatin Remodeling Complexes in Pancreatic Cancer
Evaluating the Pathogenic Potential of Genes with De Novo Variants in Epileptic Encephalopathies
ATP-Dependent Chromatin Remodeler CHD9 Controls the Proliferation of Embryonic Stem Cells in a Cell Culture Condition-Dependent Manner
The Role of Hud in Alternative Splicing and Alternative Polyadenylation in the Brain
New SMARCA2 Mutation in a Patient with Nicolaides-Baraitser Syndrome