Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Cecilia S. L. Lai"'
Autor:
Cecilia S. L. Lai, Victor Wiebe, Takashi Kitano, Simon E. Fisher, Anthony P. Monaco, Wolfgang Enard, Molly Przeworski, Svante Pääbo
Publikováno v:
Nature. 418:869-872
Language is a uniquely human trait likely to have been a prerequisite for the development of human culture. The ability to develop articulate speech relies on capabilities, such as fine control of the larynx and mouth, that are absent in chimpanzees
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c33efc577eb97facd3e01fc4b8867ac
https://doi.org/10.1038/nature01025
https://doi.org/10.1038/nature01025
Publikováno v:
Nature. 413:519-523
Individuals affected with developmental disorders of speech and language have substantial difficulty acquiring expressive and/or receptive language in the absence of any profound sensory or neurological impairment and despite adequate intelligence an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d027d8c1a1c63d506fe3289ff6aa89d2
https://doi.org/10.1038/35097076
https://doi.org/10.1038/35097076
Autor:
Robert L. Smith, Elena Bonora, Fiona Haslam McKenzie, Kay D. MacDermot, Anne Marie Coupe, Sonja C. Vernes, Simon E. Fisher, Nuala Sykes, Cecilia S. L. Lai, Faraneh Vargha-Khadem, Anthony P. Monaco
Publikováno v:
American Journal of Human Genetics
FOXP2, the first gene to have been implicated in a developmental communication disorder, offers a unique entry point into neuromolecular mechanisms influencing human speech and language acquisition. In multiple members of the well-studied KE family,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55b695581810c391830031321112e865
https://pubmed.ncbi.nlm.nih.gov/15877281
https://pubmed.ncbi.nlm.nih.gov/15877281
Publikováno v:
Annual Review of Neuroscience
▪ Abstract A significant number of individuals have unexplained difficulties with acquiring normal speech and language, despite adequate intelligence and environmental stimulation. Although developmental disorders of speech and language are heritab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff26508858ccf42de0d10283afdf3d04
https://pubmed.ncbi.nlm.nih.gov/12524432
https://pubmed.ncbi.nlm.nih.gov/12524432
Autor:
Jane A. Hurst, Shirley Hodgson, Simon E. Fisher, D. Curtis Jamison, Margaret Fox, Elaine R. Levy, Susan Povey, Faraneh Vargha-Khadem, Cecilia S. L. Lai, Stephen Jeremiah, Anthony P. Monaco, Eric D. Green
Publikováno v:
American Journal of Human Genetics
The KE family is a large three-generation pedigree in which half the members are affected with a severe speech and language disorder that is transmitted as an autosomal dominant monogenic trait. In previously published work, we localized the gene res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02589303e760478c75e36a7397a07888
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1287211&tool=pmcentrez&rendertype=abstract
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1287211&tool=pmcentrez&rendertype=abstract
Publikováno v:
Brain: A Journal of Neurology; 11/1/2003, Vol. 126 Issue 11, p2455, 8p