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ARHGEF9
The University of Chicago Genetic Services Laboratories
Fig. S1
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Table of Contents Neurology.Org/Ng Online ISSN: 2376-7839 Volume 3, Number 3, June 2017
Supplemental Information
Whole Exome Sequencing in Families at High Risk for Hodgkin Lymphoma: Identification of a Predisposing Mutation in the KDR Gene
Mutation P.R356Q in the Collybistin Phosphoinositide Binding Site Is Associated with Mild Intellectual Disability
ARHGEF9 Mutations in Epileptic Encephalopathy/Intellectual Disability: Toward Understanding the Mechanism Underlying Phenotypic Variation
Characterization of X-Linked SNP Genotypic Variation in Globally Distributed Human Populations Genome Biology 2010, 11:R10
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An Introduction to Neurogenetics
A Novel Ribosomopathy Caused by Dysfunction of RPL10 Disrupts Neurodevelopment and Causes X-Linked Microcephaly in Humans
Supporting Information
Missense Mutation R338W in ARHGEF9 in a Family with X-Linked Intellectual Disability with Variable Macrocephaly and Macro-Orchidism
Comprehensive Analysis of Coding Variants Highlights Genetic Complexity in Developmental and Epileptic Encephalopathy
Rho Gtpase Regulators and Effectors in Autism Spectrum Disorders
ARHGEF9 (3): Sc-136393
Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes
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Identification of Blood Biomarkers for Psychosis Using Convergent
Phenotypes and Variants in Cases Submitted for X-Linked Intellectual Disability (XLID) Gene Panel Testing
S41467-019-13144-Y.Pdf
A Molecular Neuroethological Approach for Identifying and Characterizing a Cascade of Behaviorally Regulated Genes
The Impact of X-Chromosome Inactivation on Phenotypic Expression of X-Linked Neurodevelopmental Disorders
The Role of Neuronal Complexes in Human X-Linked Brain Diseases
Neonatal Thyroxine Activation Modifies Epigenetic Programming of the Liver
A Genome-Wide Positioning Systems Network Algorithm for in Silico Drug Repurposing
Downloaded from NCBI SRA to Quantify Translation Levels from the Uorfs and Anorfs and To
An Integer Programming Framework for Inferring Disease Complexes from Network Data Arnon Mazza1, Konrad Klockmeier2, Erich Wanker2 and Roded Sharan1,*
Xq11.1-11.2 Deletion Involving ARHGEF9 in a Girl with Autism Spectrum Disorder
Convergent Functional Genomic Studies of Omega-3 Fatty Acids in Stress Reactivity, Bipolar Disorder and Alcoholism
The Role of Gephyrin, Collybistin and Novel Gefs in the Synaptic Clustering of Inhibitory Receptors
ARHGEF9 (N-12): Sc-167129
Supplemental Information.Pdf
ARHGEF9 Disease Phenotype Clarification and Genotype-Phenotype Correlation
Genomic Aberrations Associated with the Pathophysiological Mechanisms of Neurodevelopmental Disorders
Description of Strs in Trinucleotide-Repeat Diseases
Activity-Dependent Changes in Gene Expression in Schizophrenia
Loss-Of-Function Mutation of Collybistin Is Responsible for X-Linked Mental Retardation Associated with Epilepsy
Sex Differences in Gene Expression in the Human Fetal Brain
1 Gephyrin, a Master Regulator of Neuronal Function?