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Clinical Biochemistry|December 1, 1979
Simultaneous occurrence of xanthine oxidase and sulfite oxidase deficiency. A molybdenum dependent inborn error of metabolism?C van der Heiden, F A Beemer, W Brink, et al.Nederlands Tijdschrift Voor Geneeskunde|July 22, 1995
[Incidence and prevalence of hemoglobinopathies in children in The Netherlands]J H Rengelink-van der Lee, T W Schulpen, F A BeemerClinical Genetics|May 1, 1983
A lethal neonatal variant of carbamoyl-phosphate synthetase deficiency in combination with an intermediate activity of L-ornithine: 2-oxoglutarate amino-transferaseC van der Heiden, F A Beemer, H A van Dijk, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|March 31, 1988
Esterase D: evaluation of a potential derived gene marker for hereditary retinoblastomaC van der Heiden, A F Geurtzen, W Brink, et al.Human Genetics|January 1, 1982
Ring chromosome 2: clinical, chromosomal, and biochemical aspectsM Jansen, F A Beemer, C van der Heiden, et al.Clinical Biochemistry|October 1, 1990
Red blood cell enzymes in the diagnosis of genetic diseaseC van der HeidenNederlands Tijdschrift Voor Geneeskunde|December 19, 1992
[The Reformed Church in Aduard: the oldest hospital in The Netherlands]P C van der HeidenNederlands Tijdschrift Voor Geneeskunde|June 12, 1998
[Genetic carrier screening for hemoglobinopathies in the Netherlands is not opportune]T W Schulpen, J H van der Lee, M W van der Most van Spijk, et al.Journal of Inherited Metabolic Disease|January 1, 1982
Spectral studies of the interaction of the substrate 'quinonoid' 6-methyl dihydropterine and the coenzyme NADH used as marker in the dihydropteridine reductase assayC van der Heiden, W BrinkEuropean Journal of Pediatrics|May 1, 1996
Migration and child health: the Dutch experienceT W SchulpenPageof 18