Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia
- Author
- FEUK, Lars1 ; KALERVO, Aino2 ; RIVLIN, Joseph9 ; ROBERTS, Wendy10 ; SENMAN, Lili10 ; SUMMERS, Anne11 ; SZATMARI, Peter12 ; WONG, Virginia13 ; VINCENT, John B14 15 ; ZEESMAN, Susan8 ; OSBORNE, Lucy R16 17 ; ORAM CARDY, Janis18 ; LIPSANEN-NYMAN, Marita3 ; KERE, Juha19 2 ; SCHERER, Stephen W13 ; HANNULA-JOUPPI, Katariina2 ; SKAUG, Jennifer1 ; NAKABAYASHI, Kazuhiko1 ; FINUCANE, Brenda4 ; HARTUNG, Danielle5 ; INNES, Micheil6 ; KEREM, Batsheva7 ; NOWACZYK, Małgorzata J8
[1] Centre for Applied Genomics and Program in Genetics and Genomic Biology, University of Toronto, Toronto, Canada
[2] Department of Medical Genetics, Biomedicum, University of Helsinki, Finland
[3] Hospital for Children and Adolescents, Helsinki, Finland
[4] Genetic Services, Elwyn, Inc, Elwyn, PA, Canada
[5] Children's Memorial Hospital, Chicago, United States
[6] Department of Medical Genetics, Alberta Children's Hospital, Calgary, Canada
[7] Department of Genetics, The Life Sciences Institute, The Hebrew University, Jerusalem, Israel
[8] Department of Pediatrics, McMaster University, Hamilton, Canada
[9] Cystic Fibrosis Center, Carmel Medical Center, Haifa, Israel
[10] The Child Development Centre, University of Toronto, Toronto, Canada
[11] The Hospital for Sick Children, the Department of Genetics, North York General Hospital, University of Toronto, Toronto, Canada
[12] Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Canada
[13] Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, University of Hong Kong, Hong-Kong
[14] Centre for Addiction and Mental Health, Clarke Institute, University of Toronto, Toronto, Canada
[15] Department of Psychiatry, University of Toronto, Toronto, Canada
[16] Department of Medicine, University of Toronto, Toronto, Canada
[17] Department of Molecular and Medical Genetics, University of Toronto, Toronto, Canada
[18] School of Communication Sciences and Disorders, University of Western Ontario, London, Canada
[19] Department of Biosciences and Nutrition and Clinical Research Center, Karolinska Institute, Stockholm, Sweden - Source
American journal of human genetics. 2006, Vol 79, Num 5, pp 965-972, 8 p ; ref : 34 ref
- Publisher
- University of Chicago Press, Chicago, IL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Dyspraxie Génétique Homme Maladie héréditaire Gène FOXP2
- Keyword (en)
- Dyspraxia Genetics Human Genetic disease FOXP2 gene
- Keyword (es)
- Dispraxia Genética Hombre Enfermedad hereditaria
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A04 Molecular and cellular biology
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23A General aspects. Genetic counseling
- Discipline
- Eukaryotes genetics. Biological and molecular evolution Medical genetics Molecular and cell biology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 18232528
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
10.1086/508902 
https://dx.doi.org/10.1086/508902
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