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CACNA2D4
Bioinformatics Tools for the Analysis of Gene-Phenotype Relationships Coupled with a Next Generation Chip-Sequencing Data Processing Pipeline
RHNO1 Bidirectional Genes in Cancer
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
NIH Public Access Author Manuscript Biochim Biophys Acta
Genome-Wide Association Study Identifies Candidate Genes
Recurrent Copy Number Changes in Mentally Retarded Children Harbour Genes Involved in Cellular Localization and the Glutamate Receptor Complex
An Integrative Genomic Analysis of the Longshanks Selection Experiment for Longer Limbs in Mice
Determining the Causes of Recessive Retinal Dystrophy
INTRODUCING a NOVEL METHOD for GENETIC ANALYSIS of AUTISM SPECTRUM DISORDER Sepideh Nouri
Downloaded from the University of California Santa Cruz (UCSC) Genome Browser Based on Mm9
CACHD1 Is an Α2δ-Like Protein That
Mitochondrial and Ion Channel Gene Alterations in Autism☆
Variable Phenotypes of Epilepsy, Intellectual Disability, And
Chromosomal Microarray Analysis in the Genetic Evaluation of 279
Whole Genome Sequencing Revealed Mutations in Two Independent Genes As the Underlying Cause of Retinal Degeneration in an Ashkenazi Jewish Pedigree
A Role for Alternative Splicing in Circadian Control of Exocytosis and Glucose Homeostasis
Spaceflight Influences Gene Expression, Photoreceptor
The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential
Top View
Prognosticating Retinal Dystrophies in the Postgenomic Era Inheritance Patterns of Retinal Diseases
Genomic Profiling Reveals Pitx2 Controls Expression of Mature
Transcriptome Analysis Identifies Novel Mechanisms Associated with the Antitumor Effect of Chitosan-Stabilized Selenium Nanopart
Metastatic Colorectal Cancer and Severe Hypocalcemia Following
Genomic Aberrations of the CACNA2D1 Gene in Three Patients with Epilepsy and Intellectual Disability
HHS Public Access HHS Public Nat Genet Nat Author Manuscript
A Novel Splice-Site Variant in CACNA1F Causes a Phenotype Synonymous with Åland Island Eye Disease and Incomplete Congenital Stationary Night Blindness