Work

Genotype, molecular phenotype, and cognitive phenotype: Correlations in fragile X syndrome

Year: 1999

Type: article

Study design: Observational Study

Source: American Journal of Medical Genetics

DOI: 10.1002/(sici)1096-8628(19990402)83:4<286::aid-ajmg10>3.0.co;2-h

Authors: Walter E. Kaufmann, Michael T. Abrams, Wilma Chen, Allan L. Reiss

Institutions: Johns Hopkins University, Johns Hopkins Medicine, Kennedy Krieger Institute, Stanford Medicine, Stanford University

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institute of Mental Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G3016495783, G3293162334, Mental Retardation and Developmental Disabilities Research Centers 2008, G5824905338, Developmental trajectory of anxiety, avoidance, and arousal in girls with the FMR1 full mutation

OpenAlex ID: W2117342187

FWCI: 4.052

Cites: 44

Cited by: 134

Related to: 10