Work

Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation

Year: 2007

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics Part A

DOI: 10.1002/ajmg.a.31781

Authors: Frank J. Probst, Elizabeth R. Roeder, Victoria B. Enciso, Zhishuo Ou, M. Lance Cooper, Patricia Eng, Jiangzhen Li, Yanghong Gu, Robert F. Stratton, A. Craig Chinault, Chad A. Shaw, V. Reid Sutton, Sau Wai Cheung, David L. Nelson

Institutions: Baylor College of Medicine, The University of Texas at San Antonio Health Science Center, Opexa Therapeutics (United States)

Language: English

Topic: Genomic variations and chromosomal abnormalities

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 Human Genome Research Institute, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G1289049516, Functional Analysis of the Mouse X Chromosome, Fragile X Related Genes Mental Retardation/Development

OpenAlex ID: W2090572207

FWCI: 3.851

Cites: 42

Cited by: 60

Related to: 10