Work

FG syndrome, an X-linked multiple congenital anomaly syndrome: The clinical phenotype and an algorithm for diagnostic testing

Year: 2009

Type: article

Study design: Observational Study

Source: Genetics in Medicine

DOI: 10.1097/gim.0b013e3181bd3d90

Authors: Robin Dawn Clark, John M. Graham, Michael J. Friez, Joe J. Hoo, Kenneth Lyons Jones, Carole McKeown, John B. Moeschler, F. Lucy Raymond, R. Curtis Rogers, Charles E. Schwartz, Agatino Battaglia, Michael J. Lyons, Roger E. Stevenson

Institutions: Loma Linda University Medical Center, Loma Linda University, Loma Linda University Health Care, Cedars-Sinai Medical Center, Greenwood Genetic Center, University of Toledo, University of California San Diego, Birmingham Women's Hospital, Dartmouth–Hitchcock Medical Center, University of Cambridge, Fondazione Stella Maris

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: U.S. Department of Health and Human Services, Action Medical Research, National Institute for Health and Care Research, National Institutes of Health, Health Resources and Services Administration, National Institute of General Medical Sciences, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G1151667499, G194938417, G199406178, The Skeletal Dysplasias, X-Linked Mental Retardation-Linkage, UCLA Medical Genetics Training Program

OpenAlex ID: W2091012403

FWCI: 1.538

Cites: 19

Cited by: 41

Related to: 10