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المؤلفون: Nudel, R., Simpson, N., Baird, G., O’Hare, A., Conti-Ramsden, G., Bolton, P., Hennessy, E., The SLli consortium, Ring, S., Smith, G., Francks, C., Paracchini, S., Monaco, A., Fisher, S., Newbury, D.
المساهمون: The Royal Society, University of St Andrews. School of Medicine, University of St Andrews. Biomedical Sciences Research Complex
المصدر: Genes, Brain and Behavior
Genes, Brain, and Behaviorمصطلحات موضوعية: Adult, Male, Genotype, Apraxias, Quantitative Trait Loci, QH426 Genetics, Polymorphism, Single Nucleotide, Genomic Imprinting, Neurodevelopmental disorder, RZ, Chromosomes, Human, Guanine Nucleotide Exchange Factors, Humans, GWAS, Child, QH426, Adaptor Proteins, Signal Transducing, Tumor Suppressor Proteins, RNA-Binding Proteins, Imprinting, Original Articles, ALSPAC, neurodevelopmental disorder, specific language impairment, Specific language impairment, RC0321, Female, imprinting, Apoptosis Regulatory Proteins, Receptors, Prostaglandin E, EP4 Subtype, RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry, Genome-Wide Association Study
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::336807296491e2f20459442ce6500f2f
https://ora.ox.ac.uk/objects/uuid:3c7de768-93bf-40f7-bff0-13bb7d05adf1