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1
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment
In: Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment (2017)
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2
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment
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3
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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4
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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5
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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6
Associations of HLA alleles with 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) (2014)
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7
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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8
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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