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Neuron, ISSN 0896-6273, 03/2016, Volume 89, Issue 6, pp. 1208 - 1222
Trisomy 21, or Down syndrome (DS), is the most common genetic cause of developmental delay and intellectual disability. To gain insight into the underlying... 
brain development | white matter | genomics | neocortex | neurodevelopmental disorders | glia | gene expression | Genomics | Brain development | Gene expression | Glia | Neocortex | Neurodevelopmental disorders | White matter | TS65DN MOUSE MODEL | DEVELOPING CNS | WHITE-MATTER | CORTEX | IN-VIVO | GENE-EXPRESSION | LONG-TERM POTENTIATION | HIPPOCAMPAL-FORMATION | MATURATION | COGNITIVE-DEVELOPMENT | NEUROSCIENCES | Action Potentials - genetics | Humans | Child, Preschool | Gene Expression Regulation, Developmental - genetics | Infant | Male | Down Syndrome - physiopathology | Gene Expression Profiling | Brain - growth & development | White Matter - ultrastructure | Chromosomes, Human, Pair 17 - genetics | Myelin Sheath - metabolism | Brain - metabolism | Myelin Basic Protein - genetics | Young Adult | Cell Differentiation - genetics | Adult | Female | Cell Differentiation - physiology | Child | Infant, Newborn | Disease Models, Animal | Down Syndrome - pathology | Myelin Basic Protein - metabolism | Myelin Sheath - pathology | Neural Conduction - genetics | Mice, Transgenic | White Matter - pathology | Oligodendroglia - pathology | Animals | Trisomy - genetics | Adolescent | Down Syndrome - genetics | Brain - pathology | Mosaicism | Mice | Myelin Sheath - ultrastructure | Postmortem Changes | Brain | Medical colleges | Down syndrome | Analysis | Neurophysiology | Anopheles | Genes | Development and progression | Neuropathology | Principal components analysis | Genomes | Alzheimers disease | Laboratory animals | Chromosomes
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