Neurocognitive functioning of a child with partial trisomy 6 and monosomy 21

This case study describes the neurocognitive presentation of a child with identified genetic abnormalities of trisomy 6 and monosomy 21 who was evaluated as part of a standard medical protocol for cochlear implantation following diagnosis of profound sensorineural hearing loss. This child received n...

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Veröffentlicht in:Neurocase 2009-01, Vol.15 (2), p.97-100
Hauptverfasser: Katzenstein, Jennifer M., Oghalai, John S., Tonini, Ross, Baker, Dian, Haymond, Jody, Caudle, Susan E.
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Sprache:eng
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