Work

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1

Year: 1998

Type: article

Study design: Observational Study

Source: Human Molecular Genetics

DOI: 10.1093/hmg/7.12.1935

Authors: C. Gunter, W. Paradee, D. C. Crawford, K. A. Meadows, J. Newman, C. B. Kunst, D. L. Nelson, C. Schwartz, A. Murray, J. N. Macpherson, S. L. Sherman, S. T. Warren

Institutions: Howard Hughes Medical Institute, Emory University, Baylor College of Medicine, Greenwood Genetic Center, Salisbury District Hospital, Wessex Regional Genetics Laboratory

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: Howard Hughes Medical Institute, National Institutes of Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G1356581462, G1535018248, G5575622741, Genetics Epidemiology of the FMR1 Gene, A PROGRAM OF INVESTIGATION INTO FRAGILE X SYNDROME

OpenAlex ID: W2129173429

FWCI: 2.653

Cites: 36

Cited by: 70

Related to: 10