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FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.
Leehey, M A; Berry-Kravis, E; Goetz, C G; Zhang, L; Hall, D A; Li, L; Rice, C D; Lara, R; Cogswell, J; Reynolds, A; Gane, L; Jacquemont, S; Tassone, F; Grigsby, J; Hagerman, R J; Hagerman, P J.
Affiliation
  • Leehey MA; Department of Neurology, University of Colorado at Denver and Health Sciences Center, Denver, CO 80262, USA. maureen.leehey@uchsc.edu
Neurology ; 70(16 Pt 2): 1397-402, 2008 Apr 15.
Article in En | MEDLINE | ID: mdl-18057320
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Trinucleotide Repeat Expansion / Fragile X Mental Retardation Protein / Fragile X Syndrome / Genetic Carrier Screening / Movement Disorders / Mutation Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Neurology Year: 2008 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Trinucleotide Repeat Expansion / Fragile X Mental Retardation Protein / Fragile X Syndrome / Genetic Carrier Screening / Movement Disorders / Mutation Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Neurology Year: 2008 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos