F. A. Beemer

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

A K Ryan, Judith A. Goodship, David I. Wilson et al. · Journal of Medical Genetics · 1997 · 1.2K citations · Full text

Cytogenetics, Genetics, Genetic Epidemiology +23

Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor.

Jean L. Johnson, William R. Waud, K.V. Rajagopalan et al. · Proceedings of the National Academy of Sciences · 1980 · 167 citations · Full text

Pathology, Molybdenum Cofactor, Plasma Molybdenum Concentration +18

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

M. Durán, F. A. Beemer, Colin van der Heiden et al. · Journal of Inherited Metabolic Disease · 1978 · 124 citations

Symptomatology of patients with oligodontia

Y. Schalk-van der Weide, F. A. Beemer, Jorge Faber et al. · Journal of Oral Rehabilitation · 1994 · 112 citations

Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism

Rolf M.F. Berger, S. A. Stoker‐de Vries, S.K. Wadman et al. · Clinica Chimica Acta · 1984 · 100 citations

Urology, Pyrimidine Metabolism, Iodine Deficiency Disorders +3