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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.Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 1975
Permanent chemical phenylketonuria and a normal phenylalanine tolerance in two sisters with a normal mental developmentS K Wadman, D Ketting, P K De Bree, et al.European Journal of Pediatrics|July 19, 1978
Attempted dietary treatment of a boy with hyperammonemia due to ornithine transferase deficiencyC van der Heiden, H D Bakker, J Desplanque, et al.Pediatric Research|October 1, 1977
Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated musclesJ P Van Biervliet, L Bruinvis, D Ketting, et al.Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|December 1, 1989
Gamma-glutamyltransferase: evaluation of a new methodC van der Heiden, J C Hafkenscheid, J van der Ven-Jongekrijg, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|May 15, 1975
Tyrosinemia and tyrosyluria in healthy prematures: time courses not vitamin C-dependentH D Bakker, S K Wadman, F J Van Sprang, et al.Archives of Neurology|January 1, 1986
Familial association of intracranial aneurysms and multiple congenital anomaliesH W ter Berg, J B Bijlsma, J A Veiga Pires, et al.Lancet (London, England)|September 17, 1988
What is the best predictor of the severity of ABO-haemolytic disease of the newborn?H A Brouwers, M A Overbeeke, I van Ertbruggen, et al.Pageof 2