F. A. Beemer

3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal

M. Durán, S. K. Wadman, K. Gibson, 1988, European Journal of Pediatrics.

Restrictive dermopathy and fetal behaviour

E. Mulder, P. Stoutenbeek, F. Beemer, 2001, Prenatal diagnosis.

Absence of hepatic molybdenum cofactor: An inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase

M. Durán, K. Rajagopalan, J. Johnson, 1983, Journal of Inherited Metabolic Disease.

Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport?

M. Durán, S. K. Wadman, F. Beemer, 1978, Journal of Inherited Metabolic Disease.

Early diagnosis of bilateral retinoblastoma reduces death and blindness

K. Tan, F. Beemer, N. Nagelkerke, 1989, International journal of cancer.

A patient with α-ketoadipic and α-aminoadipic aciduria

M. Durán, U. Wendel, S. K. Wadman, 1984, Journal of Inherited Metabolic Disease.

Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs

M. Durán, D. Ketting, S. K. Wadman, 1982, European Journal of Pediatrics.

Ring chromosome 2: Clinical, chromosomal, and biochemical aspects

F. Beemer, J. L. Brande, M. Jansen, 2004, Human Genetics.