Work

Prenatal diagnosis of multiple acyl‐CoA dehydrogenase deficiency: association with elevated α‐fetoprotein and cystic renal changes

Year: 2001

Type: article

Study design: Case Report

Source: Prenatal Diagnosis

DOI: 10.1002/pd.157

Authors: Christian A. Chisholm, Fotini Vavelidis, Mark A. Lovell, Lawrence Sweetman, Charles R. Roe, Diane S. Roe, Frank E. Frerman, William G. Wilson

Institutions: University of Virginia, Baylor University Medical Center, University of Colorado Anschutz, University of Colorado Denver

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G1678678574, GENETIC BIOCHEMICAL DISORDERS IN MENTAL RETARDATION

OpenAlex ID: W1966532246

FWCI: 0.558

Cites: 12

Cited by: 17

Related to: 10