Genotype, molecular phenotype, and cognitive phenotype: correlations in fragile X syndrome.

Kaufmann, W E; Abrams, M T; Chen, W; Reiss, A L

Kaufmann, W E; Abrams, M T; Chen, W; Reiss, A L.

Affiliation

Kaufmann WE; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA. wekaufma@welchlink.welch.jhu.edu

Am J Med Genet ; 83(4): 286-95, 1999 Apr 02.

Article in En | MEDLINE | ID: mdl-10208163

Subject(s)

Cognition; Fragile X Syndrome/metabolism; Fragile X Syndrome/psychology; Nerve Tissue Proteins; RNA-Binding Proteins; Adolescent; Adult; Animals; Child; Child, Preschool; Fragile X Mental Retardation Protein; Fragile X Syndrome/genetics; Genotype; Haplorhini; Humans; Immunoblotting; Intelligence Tests; Nerve Tissue Proteins/genetics; Nerve Tissue Proteins/immunology; Nerve Tissue Proteins/metabolism; Phenotype

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Database: MEDLINE Main subject: RNA-Binding Proteins / Cognition / Fragile X Syndrome / Nerve Tissue Proteins Type of study: Prognostic_studies Limits: Adolescent / Adult / Animals / Child / Child, preschool / Humans Language: En Year: 1999 Type: Article

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