Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene
- Author
- PEYRARD-JANVID, Myriam1 ; ANTHONI, Heidi1 ; KERE, Juha1 4 ; ONKAMO, Päivi2 ; LAHERMO, Päivi3 ; ZUCCHELLI, Marco1 ; KAMINEN, Nina4 ; HANNULA-JOUPPI, Katariina4 ; NOPOLA-HEMMI, Jaana4 5 6 ; VOUTILAINEN, Arja5 ; LYYTINEN, Heikki7
[1] Department of Biosciences at NOVUM, Karolinska Institutet, 141 57 Huddinge, Sweden
[2] HIIT-BRU, Department of Computer Science, University of Helsinki, Helsinki, Finland
[3] Finnish Genome Center, University of Helsinki, Helsinki, Finland
[4] Department of Medical Genetics, Biomedicum, University of Helsinki, Helsinki, Finland
[5] Department of Pediatric Neurology, Hospital for Children and Adolescents, University of Helsinki, Helsinki, Finland
[6] Department of Pediatrics, Jorvi Hospital, Espoo, Finland
[7] Department of Psychology and Child Research Center, University of Jyväskylä, Jyväskylä, Finland - Source
Human genetics. 2004, Vol 114, Num 5, pp 510-516, 7 p ; ref : 25 ref
- CODEN
- HUGEDQ
- ISSN
- 0340-6717
- Scientific domain
- Biotechnology; Genetics
- Publisher
- Springer, Berlin
/
Springer, Heidelberg
/
Springer, New York, NY
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Carte génétique Dyslexie Gène candidat Génétique Locus Système nerveux pathologie Trouble communication Trouble langage Trouble lecture Trouble neurologique
- Keyword (en)
- Genetic mapping Dyslexia Candidate gene Genetics Locus Nervous system diseases Communication disorder Language disorder Reading disorder Neurological disorder
- Keyword (es)
- Mapa genético Dislexia Gen candidato Genética Locus Sistema nervioso patología Trastorno comunicación Trastorno lenguaje Trastorno lectura Trastorno neurológico
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution / 002A07C Classical genetics, quantitative genetics, hybrids / 002A07C03 Human
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution / 002A07C Classical genetics, quantitative genetics, hybrids / 002A07C04 Methods, theories and miscellaneous
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A02 Disorders of higher nervous function. Focal brain diseases. Central vestibular syndrome and deafness. Brain stem syndromes
- Discipline
- Eukaryotes genetics. Biological and molecular evolution Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 15648530
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1007/s00439-004-1103-0 
https://dx.doi.org/10.1007/s00439-004-1103-0
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