Continuing Commentary
Why are adoptees so similar in IQ?
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- 19 May 2011, p. 336
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Why children in the same family are so different from one another
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- 19 May 2011, pp. 336-338
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Continuing Commentary
Predicting from the right shift theory
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- 19 May 2011, pp. 338-341
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Human handedness reconsidered
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- 19 May 2011, pp. 341-342
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It's all in the hands of the beholder: New data on free-ranging rhesus monkeys
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- 19 May 2011, pp. 342-344
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Author's Response
Primate handedness: The other theory, the other hand and the other attitude
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- 19 May 2011, pp. 344-349
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Continuing Commentary
Sensory templates: Mechanism or metaphor?
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- 19 May 2011, pp. 349-350
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Ab ovo with song!
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- 19 May 2011, pp. 350-351
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Instinct and innateness: Information in causes
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- 19 May 2011, p. 351
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Author's Response
On the unmodifiability of views and the innateness of behavior
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- 19 May 2011, pp. 351-352
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Continuing Commentary
Potential difficulties in the evaluation of motor strategies using EMG patterns
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- 19 May 2011, pp. 352-353
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Motor strategy selection by cognitive controllers
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- 19 May 2011, pp. 353-354
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Network relaxation as biological computation
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- 19 May 2011, pp. 354-356
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Are there multiple movement strategies?
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- 19 May 2011, p. 356
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The issue of motor equivalence
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- 19 May 2011, pp. 356-357
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Strategies for the control of voluntary movements in patients with Parkinson's disease
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- 19 May 2011, p. 357
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Strategies for goal-directed fast movements are byproducts of satisfying performance criteria
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- 19 May 2011, pp. 357-359
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Author's Response
Movement strategies and the necessity for task differentiation
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- 19 May 2011, pp. 359-364
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Continuing Commentary
Haunted by the specter of creole genesis
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- 19 May 2011, pp. 364-366
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Author's Response
Simple triggers and creoles
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- 19 May 2011, pp. 366-368
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