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 |
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Format: | Artikel |
Sprache: | eng |
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