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Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.
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In: ISSN: 1553-7390 ; EISSN: 1553-7404 ; PLoS Genetics ; https://www.hal.inserm.fr/inserm-00715268 ; PLoS Genetics, Public Library of Science, 2011, 7 (7), pp.e1002145. ⟨10.1371/journal.pgen.1002145⟩ (2011)
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Auditory cortical N100 in pre- and post-synaptic auditory neuropathy to frequency or intensity changes of continuous tones.
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In: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, vol 122, iss 3 (2011)
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Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration
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Triagem auditiva neonatal: das alterações auditivas à análise molecular Newborn hearing screening: from audiological alterations to molecular analyses
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In: Revista CEFAC, Vol 13, Iss 5, Pp 909-916 (2011) (2011)
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Semantic Mutation Testing
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In: http://www.cs.york.ac.uk/%7Ejac/PublishedPapers/semantic_journal4.pdf (2010)
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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
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In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, vol 153B, iss 4 (2010)
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Kırgız Türkçesindeki Rusça Alıntı Sözcükler ve Bu Sözcüklerdeki Ünsüz Olayları
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In: Zeitschrift für die Welt der Türken / Journal of World of Turks; Vol 2, No 2 (2010): [ZfWT] Vol. 2, No. 2 (2010); 227-241 (2010)
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Syndromes of nonfluent primary progressive aphasia A clinical and neurolinguistic analysis
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In: NEUROLOGY , 75 (7) 603 - 610. (2010) (2010)
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Phonology Shaped by Phonetics: The Case of Intervocalic Lenition
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Nucleotide modifications in three functionally important regions of the Saccharomyces cerevisiae ribosome affect translation accuracy.
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In: ISSN: 0305-1048 ; EISSN: 1362-4962 ; Nucleic Acids Research ; https://hal.archives-ouvertes.fr/hal-00527402 ; Nucleic Acids Research, Oxford University Press, 2009, 37 (22), pp.7665-77. ⟨10.1093/nar/gkp816⟩ (2009)
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ХАРАКТЕР ОБУСЛОВЛЕННОСТИ СТЕПЕНИ СЕМАНТИЧЕСКОГО ОТРЫВА ОМОНИМОВ В АДЪЕКТИВНЫХ СЛОВООБРАЗОВАТЕЛЬНЫХ ОМОНИМИЧЕСКИХ РЯДАХ
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Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals.
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In: Brain research, vol 1300 (2009)
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FOXP2 as a molecular window into speech and language.
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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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Unravelling neurogenetic networks implicated in developmental language disorders.
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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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Investigação genética da surdez hereditária: mutação do gene da Conexina 26 Genetic investigation of hereditary deafness: connexin 26 gene mutation
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In: Revista da Sociedade Brasileira de Fonoaudiologia, Vol 14, Iss 1, Pp 142-147 (2009) (2009)
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Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
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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 (2008)
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Mapping cortical thickness in children with 22q11.2 deletions
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In: http://cercor.oxfordjournals.org/content/17/8/1889.full.pdf (2007)
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Mapping cortical thickness in children with 22q11.2 deletions
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In: http://cercor.oxfordjournals.org/content/early/2006/10/20/cercor.bhl097.full.pdf (2007)
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Mapping cortical thickness in children with 22q11.2 deletions
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In: http://www.ucdmc.ucdavis.edu/mindinstitute/research/cabil/publications/simon22q-cort-thickness.pdf (2007)
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