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Acta Biologica Et Medica Germanica|January 1, 1982
[Resorption disorders in children with phenylketonuria]G Cobet, K BeyreissPsychiatrie, Neurologie, Und Medizinische Psychologie|March 1, 1990
[Biotinidase deficiency--a progressive metabolic disease in children with seizures and ataxia]H Anger, K Lorenz, G CobetPadiatrie Und Grenzgebiete|January 1, 1993
[Dietary management of phenylketonuria patients using a personal computer]G Cobet, U Creutzburg, G Siebert, et al.Clinical Genetics|October 1, 1987
Introduction of genomic diagnosis of classical phenylketonuria to the health care system of the German Democratic RepublicO Riess, A Michel, A Speer, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|January 15, 1979
Creatine kinase isoenzyme BB in serum of healthy adults and childrenK Jung, R Neumann, G Cobet, et al.Prenatal Diagnosis|April 1, 1996
Assessment of serum levels of alpha-1-microglobulin, beta-2-microglobulin, and retinol binding protein in the fetal blood. A method for prenatal evaluation of renal functionG Cobet, T Gummelt, R Bollmann, et al.Zentralblatt Fur Gynakologie|January 1, 1994
[Cystic kidney dysplasia of variable expression--prenatal ultrasound, cytogenetic and patho-anatomic findings based on 3 case examples]C Tennstedt, R Bollmann, R Chaoui, et al.Padiatrie Und Grenzgebiete|January 1, 1993
[Partial monosomy 21 or fetal alcohol embryopathy in a retarded boy?]J Müller, G Cobet, G Laske, et al.Human Genetics|April 1, 1988
Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic RepublicO Riess, A Michel, A Speer, et al.Prenatal Diagnosis|May 1, 1991
Cu/Zn superoxide dismutase quantification from fetal erythrocytes--an efficient confirmatory test for Down's syndrome after maternal serum screening and sonographic investigationsT Porstmann, R Wietschke, G Cobet, et al.Pageof 2