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Contactin 4
Supplementary Table 1: Adhesion Genes Data Set
Gene Discovery in Developmental Neuropsychiatric Disorders : Clues from Chromosomal Rearrangements Thomas V
The Human Genome Diversity and the Susceptibility to Autism Spectrum Disorders
Nanomechanics of Ig-Like Domains of Human Contactin (BIG-2)
Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family
Supplementary Information Contents
Predicting a Double Mutant in the Twilight Zone of Low Homology
3P26 Deletions FTNW
Molecular Sciences High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorder
And Post-Synaptic Abnormalities in Schizophrenia Lynsey S
Association Study of 167 Candidate Genes for Schizophrenia Selected by a Multi-Domain Evidence- Based Prioritization Algorithm and Neurodevelopmental Hypothesis
Genetic Screening Reveals a Link Between Wnt Signaling and Antitubulin Drugs
Novel Copy Number Variants in Children with Autism and Additional Developmental Anomalies
Gene List.Pdf
Universidade Presbiteriana Mackenzie Centro De Cienciâs Biológicas E Da Saúde Curso De Ciências Biológicas
No Evidence for Association of Autism with Rare
Mapping the Genetics of Neuropsychological Traits to The
Investigating the Effects of Copy Number Variants on Reading and Language Performance Alessandro Gialluisi1,2, Alessia Visconti3, Erik G
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A Novel Splice Variant of the Cell Adhesion Molecule Contactin 4 (CNTN4) Is Mainly Expressed in Human Brain
Panels, Mini-Panels and Study Groupsdecember 4
216141 2 En Bookbackmatter 461..490
Association Study of 167 Candidate Genes for Schizophrenia Selected
Molecular Genetic Characterization of Ataxic Movement Disorders in Mouse and Human
And Chimpanzee-Specific Cytogenetic Structures
Single Gene Microdeletions and Microduplication of 3P26.3 in Three
CNTN6 Mutations Are Risk Factors for Abnormal Auditory Sensory Perception in Autism Spectrum Disorders
Penn Medicine
Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders from the South of Brazil
No Evidence for Association of Autism with Rare Heterozygous Point
Contactin 4, -5 and -6 Differentially Regulate Neuritogenesis While They Display Identical PTPRG Binding Sites
Betel-Nut)-Induced Whole Transcriptome Changes in a Human Monocyte Cell Line That May Have Relevance to Diabetes and Obesity; a Pilot Study Shirleny R Cardosa1†, B
Disruption of Contactin 4 in Three Subjects with Autism Spectrum
Mediates Genetic Susceptibility to Chronic Kidney Disease
CNTN6 Copy Number Variations in 14 Patients: a Possible Candidate Gene
Copy Number Variations and Cognitive Phenotypes in Unselected Populations
Contactin 4, -5 and -6 Differentially Regulate Neuritogenesis While They Display Identical PTPRG Binding Sites
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