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المؤلفون: Cecilia Marino, Roberto Giorda, Andrea Facoetti, Monica Consonni, Pasquale Anthony Della Rosa, Maria Luisa Lorusso, Jeffrey R. Gruen, Andrea Falini, Daniela Perani, Massimo Molteni, Paola Scifo, Sara Mascheretti
المساهمون: Marino, C, Scifo, P, Della Rosa, Pa, Mascheretti, S, Facoetti, A, Lorusso, Ml, Giorda, R, Consonni, M, Falini, Andrea, Molteni, M, Gruen, Jr, Perani, DANIELA FELICITA L.
المصدر: Cortex (Testo stamp.) 57 (2014): 227–243. doi:10.1016/j.cortex.2014.04.016
info:cnr-pdr/source/autori:Marino, Cecilia; Scifo, Paola; Della Rosa, Pasquale A.; Mascheretti, Sara; Facoetti, Andrea; Lorusso, Maria L.; Giorda, Roberto; Consonni, Monica; Falini, Andrea; Molteni, Massimo; Gruen, Jeffrey R.; Perani, Daniela/titolo:The DCDC2%2Fintron 2 deletion and white matter disorganization: Focus on developmental dyslexia/doi:10.1016%2Fj.cortex.2014.04.016/rivista:Cortex (Testo stamp.)/anno:2014/pagina_da:227/pagina_a:243/intervallo_pagine:227–243/volume:57مصطلحات موضوعية: Adult, Male, DCDC2, medicine.medical_specialty, Genu of the corpus callosum, Adolescent, Developmental dyslexia, Cognitive Neuroscience, Splenium, Experimental and Cognitive Psychology, Audiology, Corpus callosum, Neuronal migration, behavioral disciplines and activities, Article, Lateralization of brain function, Dyslexia, White matter, Young Adult, mental disorders, Fractional anisotropy, medicine, Humans, Inferior longitudinal fasciculus, READ1, Diffusion tensor imaging, medicine.disease, White Matter, Introns, Neuropsychology and Physiological Psychology, medicine.anatomical_structure, Reading, Female, Nerve Net, Psychology, Microtubule-Associated Proteins, Neuroscience
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4402cf8cf8e524346742eeae9855a349Test
https://doi.org/10.1016/j.cortex.2014.04.016Test -
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المؤلفون: Roberto Giorda, Sara Mascheretti, Maria Rosaria Cellino, Cecilia Marino, Silvana Beri, Valentina Riva, Lara Francesca Emilia Lanzoni
المصدر: Journal of human genetics. 59(4)
مصطلحات موضوعية: Proband, medicine.medical_specialty, Adolescent, Nerve Tissue Proteins, Biology, Quantitative trait locus, Language Development, Polymorphism, Single Nucleotide, Developmental psychology, Cohort Studies, Dyslexia, Cognition, Genetics, medicine, Humans, Receptors, Immunologic, Child, Nuclear family, Genetics (clinical), Genetic Association Studies, Language, Genetic Pleiotropy, Transmission disequilibrium test, Mathematical Concepts, medicine.disease, Developmental disorder, Phenotype, Genetic epidemiology, Reading, Trait, Medical genetics
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::826442afb179b0f9300a481d7078872dTest
https://pubmed.ncbi.nlm.nih.gov/24430574Test