Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.
A locus on chromosome 2p12-16 has been implicated in dyslexia susceptibility by two independent linkage studies, including our own study of 119 nuclear twin-based families, each with at least one reading-disabled child. Nonetheless, no variant of any gene has been reported to show association with d...
Κύριοι συγγραφείς: | Francks, C, Fisher, S, Olson, R, Pennington, B, Smith, S, DeFries, J, Monaco, A |
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Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
2002
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Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
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Identification of candidate genes for dyslexia susceptibility on chromosome 18.
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Correction: identification of candidate genes for dyslexia susceptibility on chromosome 18.
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Correction: Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18.
ανά: Thomas S. Scerri, κ.ά.
Έκδοση: (2010-01-01)