Work

Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA

Year: 2009

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1016/j.ajhg.2009.09.007

Authors: Bradford Coffee, Krayton Keith, Igor Albizua, Tamika Malone, Julie Mowrey, Stephanie L. Sherman, Stephen T. Warren

Institution: Emory 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: bronze

Funders: Association of American Medical Colleges, National Institutes of Health, Centers for Disease Control and Prevention, U.S. Public Health Service, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G2928211173, Molecular Cloning of the Fragile X Site, Baylor Intellectual and Developmental Disabilities Research Center, G5507216782, MOLECULAR CLONING OF THE FRAGILE X SITE

OpenAlex ID: W2106750209

FWCI: 14.39

Cites: 55

Cited by: 432

Related to: 10