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1
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
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2
The neuronal migration hypothesis of dyslexia: a critical evaluation 30 years on
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3
The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on
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4
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
In: Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes (2016)
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5
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes
In: Symplectic Elements at Oxford ; Added by author ; ORA review team (2016)
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6
Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes.
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7
Genome-wide screening for DNA variants associated with reading and language traits
Gialluisi, A; Newbury, D F; Wilcutt, E G. - : Blackwell Publishing Ltd, 2014
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8
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2014)
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9
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2014)
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10
Genome-wide screening for DNA variants associated with reading and language traits.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2014)
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11
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2014)
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12
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2014)
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13
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2014)
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14
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2014)
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15
Genome‐wide association analyses of child genotype effects and parent‐of‐origin effects in specific language impairment
Nudel, R.; Simpson, N. H.; Baird, G.. - : Blackwell Publishing Ltd, 2014
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16
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
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17
DCDC2, KIAA0319 and CMIP are associated with reading-related traits
In: Symplectic Elements at Oxford ; Scopus (http://www.scopus.com/home.url) (2011)
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18
DCDC2, KIAA0319 and CMIP are associated with reading-related traits.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2011)
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19
Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2011)
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20
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2009)
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