Work

FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome

Year: 1999

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics

DOI: 10.1002/(sici)1096-8628(19990101)82:1<25::aid-ajmg5>3.0.co;2-y

Authors: Michael T. Abrams, Walter E. Kaufmann, Fran�ois Rousseau, Ben A. Oostra, Benjamin Wolozin, Christopher V. Taylor, Nancy Lishaa, Marie-Lou Morel, Andre Hoogeveen, Allan L. Reiss

Institutions: Kennedy Krieger Institute, Johns Hopkins University, Johns Hopkins Medicine, Hôpital Saint-François d'Assise, Erasmus University Rotterdam, Loyola University Medical Center, 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 Institutes of Health, National Institute of Mental Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: ANATOMY OF REGULATORY GENES IN FOREBRAIN DEVELOPMENT, G3293162334, G3490007217, G5824905338, Developmental trajectory of anxiety, avoidance, and arousal in girls with the FMR1 full mutation

OpenAlex ID: W2161946113

FWCI: 1.937

Cites: 54

Cited by: 34

Related to: 10