Work

Tissue heterogeneity of the FMR1 mutation in a high‐functioning male with fragile X syndrome

Year: 1999

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics

DOI: 10.1002/(sici)1096-8628(19990528)84:3<233::aid-ajmg14>3.3.co;2-y

Authors: Annette K. Taylor, Flora Tassone, Pamela N. Dyer, Steven M. Hersch, Jennifer B. Harris, William T. Greenough, Randi J. Hagerman

Institutions: Emory University, University of Illinois Urbana-Champaign, University of Illinois System

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, U.S. Public Health Service, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G257707920, G5575622741, A PROGRAM OF INVESTIGATION INTO FRAGILE X SYNDROME

OpenAlex ID: W4239532046

FWCI: 3.206

Cites: 32

Cited by: 85

Related to: 10