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CENTG2
Nuclear and Mitochondrial Genome Defects in Autisms
AGAP1 (NM 014914) Human Recombinant Protein Product Data
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Targeted Resequencing Identifies Genes with Recurrent Variation In
Targeting PH Domain Proteins for Cancer Therapy
Human-Specific Gain of Function in a Developmental Enhancer
Advances in Autism Genetics: on the Threshold of a New Neurobiology
Edinburgh Research Explorer
Identification and Characterisation of Rare CACNG5 Genetic Variants in Bipolar Disorder and Schizophrenia
UNIVERSITY of CALIFORNIA, SAN DIEGO the Proteome of Mouse
Accelerated Rate of Gene Gain and Loss in Primates
Genome Variation, Diversity and Evolution
Quantitative Profiling of Peptides from Rnas Classified As Noncoding
IMFAR 09 Abstract Patrick Johnston
The 2Q37-Deletion Syndrome: an Update of the Clinical Spectrum Including Overweight, Brachydactyly and Behavioural Features in 14 New Patients
Clinical Relevance of Small Copy-Number Variants in Chromosomal Microarray Clinical Testing
Forces Shaping the Fastest Evolving Regions in the Human Genome
Molecular Sciences High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorder
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See Christopher W. Bartlett's Curriculum Vitae
Supplementary Data
Paracentric Inversion of Chromosome 2 Associated with Cryptic Duplication of 2Q14 and Deletion of 2Q37 in a Patient with Autism
Gene Expression for HIV-Associated Dementia and HIV Encephalitis in Microdissected Neurons 1: Preliminary Analysis
Chromosomal Microarray Chromosomal Microarray
Baraminic Analysis of Archaic and Modern Human Genomes
2Q37 Deletions Adults & Adolescents FTNW
Common Variants on Chromosome 6P22.1 Are Associated with Schizophrenia
Table of Contents
Quantitative Profiling of Peptides from Rnas Classified As Noncoding
216141 2 En Bookbackmatter 461..490
Mir-137, Schizophrenia, and Sleep Regulation in Drosophila Melanogaster
The DNA Sequence and Comparative Analysis of Human Chromosome 10
Human-Specific Gain of Function in a Developmental Enhancer
Contents INTRODUCTION
High-Throughput Semi-Quantitative Analysis of Insertional Mutations in Heterogeneous Tumors
HHS Public Access Provided by Caltech Authors Author Manuscript
Genome-Wide Cross-Species Analysis Linking Open Chromatin, Differential Expression
CENTG2 (Human) Recombinant Protein (P01)
(12) United States Patent (10) Patent No.: US 8,568,974 B2 Willman Et Al
A Combined Approach on the Impact of EP300 Overexpression on Drug Resistance, Invasion and Stemness in Breast Cancer
Evaluation of the Chromosome 2Q37. 3 Gene CENTG2 As an Autism Susceptibility Gene
Elucidation of Mechanisms in Mammary Tumorigenesis and Identification of Driving Events and Susceptibility Loci
Atlas Journal
Convergent Evolution of Amino Acids
Exome Sequencing of Extended Families with Autism Reveals Genes
Genetic Influences on Preterm Birth Jevon Plunkett Washington University in St