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Scale-Dependent Coding of the Hippocampus in Relational Memory
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Outgoing claims: the papers this work cites, builds on, or argues with.
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inferredcites →https://doi.org/10.1523/jneurosci.10-02-00420.1990openalex-snapshot
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inferredcites →https://doi.org/10.1523/jneurosci.17-18-07103.1997openalex-snapshot
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inferredcites →https://doi.org/10.1523/jneurosci.18-05-01841.1998openalex-snapshot
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inferredcites →https://doi.org/10.1523/jneurosci.19-05-01736.1999openalex-snapshot
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inferredcites →https://doi.org/10.5860/choice.31-5148openalex-snapshot
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Processing of different spatial scales in the human brain
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