Evaluation of the association between polymorphisms at the DRD2 locus and stuttering
スポンサーリンク
概要
- 論文の詳細を見る
- 2011-06-01
著者
-
Drayna Dennis
National Institute On Deafness And Other Communication Disorders National Institutes Of Health
-
Kang Changsoo
National Institute On Deafness And Other Communication Disorders National Institutes Of Health
-
Domingues Carlos
Department Of Genetics Bioscience Institute Sao Paulo State University (unesp)
-
Moretti-ferreira Danilo
Department Of Genetics Bioscience Institute Sao Paulo State University (unesp)
-
DOMINGUES Bianca
Department of Genetics, Bioscience Institute, Sao Paulo State University (Unesp)
-
SAINZ Eduardo
National Institute on Deafness and Other Communication Disorders, National Institutes of Health
-
Domingues Bianca
Department Of Genetics Bioscience Institute Sao Paulo State University (unesp)
-
Sainz Eduardo
National Institute On Deafness And Other Communication Disorders National Institutes Of Health
関連論文
- Characterization of a mutation commonly associated with persistent stuttering: evidence for a founder mutation
- THE SEARCH FOR THE WERNER SYNDROME GENE
- Evaluation of the association between polymorphisms at the DRD2 locus and stuttering
- Characterization of a mutation commonly associated with persistent stuttering : evidence for a founder mutation