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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Page: 1 2 3 4 5 6 Hits 61 – 80 of 106 61 Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. Vernes, Sonja,; Oliver, Peter,; Spiteri, Elizabeth... 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) BASE Show details 62 Auditory cortical N100 in pre- and post-synaptic auditory neuropathy to frequency or intensity changes of continuous tones. Dimitrijevic, Andrew; Starr, Arnold; Bhatt, Shrutee... In: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, vol 122, iss 3 (2011) BASE Show details 63 Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration B. Borroni; C. Bonvicini; D. Galimberti. - 2011 BASE Show details 64 Triagem auditiva neonatal: das alterações auditivas à análise molecular Newborn hearing screening: from audiological alterations to molecular analyses Jaqueline Medeiros de Mello; Ana Maria Silveira Machado de Moraes; Jeferson Cedaro de Mendonça... In: Revista CEFAC, Vol 13, Iss 5, Pp 909-916 (2011) (2011) BASE Show details 65 Semantic Mutation Testing John A. Clark; Haitao Dan; Robert M. Hierons In: http://www.cs.york.ac.uk/%7Ejac/PublishedPapers/semantic_journal4.pdf (2010) BASE Show details 66 Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. Ching, Michael SL; Shen, Yiping; Tan, Wen-Hann... 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) BASE Show details 67 Kırgız Türkçesindeki Rusça Alıntı Sözcükler ve Bu Sözcüklerdeki Ünsüz Olayları Mehmet ÖZEREN 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) BASE Show details 68 Syndromes of nonfluent primary progressive aphasia A clinical and neurolinguistic analysis Rohrer, JD; Rossor, MN; Warren, JD In: NEUROLOGY , 75 (7) 603 - 610. (2010) (2010) BASE Show details 69 Phonology Shaped by Phonetics: The Case of Intervocalic Lenition Kaplan, Abby. - 2010 BASE Show details 70 Nucleotide modifications in three functionally important regions of the Saccharomyces cerevisiae ribosome affect translation accuracy. Baudin-Baillieu, Agnès; Fabret, Céline; Liang, Xue-Hai... 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) BASE Show details 71 ХАРАКТЕР ОБУСЛОВЛЕННОСТИ СТЕПЕНИ СЕМАНТИЧЕСКОГО ОТРЫВА ОМОНИМОВ В АДЪЕКТИВНЫХ СЛОВООБРАЗОВАТЕЛЬНЫХ ОМОНИМИЧЕСКИХ РЯДАХ Демидова, Карелия; Батакова, Марианна. - : Государственное образовательное учреждение высшего профессионального образования Южно-Уральский государственный университет, 2009 BASE Show details 72 Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals. Huang, Taosheng; Santarelli, Rosamaria; Starr, Arnold In: Brain research, vol 1300 (2009) BASE Show details 73 FOXP2 as a molecular window into speech and language. Fisher, SE; Scharff, C 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) BASE Show details 74 Unravelling neurogenetic networks implicated in developmental language disorders. Vernes, SC; Fisher, SE 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) BASE Show details 75 Investigação genética da surdez hereditária: mutação do gene da Conexina 26 Genetic investigation of hereditary deafness: connexin 26 gene mutation Paula Michele da Silva Schmidt; Tania Maria Tochetto In: Revista da Sociedade Brasileira de Fonoaudiologia, Vol 14, Iss 1, Pp 142-147 (2009) (2009) BASE Show details 76 Lenition and fortition Carvalho, Joaquim Brandao de; Scheer, Tobias; Ségéral, Philippe. - Berlin [u.a.] : de Gruyter, 2008 MPI-SHH Linguistik Show details 77 Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Groszer, M; Keays, DA; Deacon, RM... 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) BASE Show details 78 Mapping cortical thickness in children with 22q11.2 deletions Carrie E. Bearden; Theo G. M. Van Erp; Rebecca A. Dutton... In: http://cercor.oxfordjournals.org/content/17/8/1889.full.pdf (2007) BASE Show details 79 Mapping cortical thickness in children with 22q11.2 deletions Carrie E. Bearden; Theo G. M. Van Erp; Rebecca A. Dutton... In: http://cercor.oxfordjournals.org/content/early/2006/10/20/cercor.bhl097.full.pdf (2007) BASE Show details 80 Mapping cortical thickness in children with 22q11.2 deletions Carrie E. Bearden; Theo G. M. Van Erp; Rebecca A. Dutton... In: http://www.ucdmc.ucdavis.edu/mindinstitute/research/cabil/publications/simon22q-cort-thickness.pdf (2007) BASE Show details Page: 1 2 3 4 5 6

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