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Molecular rulers for calibrating phenotypic effects of telomere imbalance
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Sotos syndrome (cerebral gigantism) - Analysis of 8 cases
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Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
P Stromme et al.
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Haploinsufficiency of NSD1 causes Sotos syndrome
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NATURE GENETICS (2002)
Disease-associated mutations in L1 CAM interfere with ligand interactions and cell-surface expression
E De Angelis et al.
HUMAN MOLECULAR GENETICS (2002)
Loss of the SKI proto-oncogene in individuals affected with 1p36 deletion syndrome is predicted by strain-dependent defects in Ski(-/-) mice
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NATURE GENETICS (2002)
X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): Clinical, magnetic resonance imaging, and neuropathological findings
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Radial glia is a progenitor developing of neocortical neurons in the cerebral cortex
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Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease
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A role for cingulate pioneering axons in the development of the corpus callosum
BG Rash et al.
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Hierarchical organization of guidance receptors: Silencing of netrin attraction by slit through a Robo/DCC receptor complex
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Neurons derived from radial glial cells establish radial units in neocortex
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NUDEL is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein
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Shape and size of the corpus callosum in schizophrenia and schizotypal personality disorder
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SCHIZOPHRENIA RESEARCH (2000)
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