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John Wiley & Sons Inc

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Familial 5q12.3 Microdeletion: Evidence for a Locus Associated with Epilepsy

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Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date

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Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome

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