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G Seidlitz

Showing results (21-30 of 48) with videos related to

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Zeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|July 1, 1983
[Homocystinuria]G Müller, H Lubs, G Seidlitz, et al.
Radiobiologia, Radiotherapia|January 1, 1976
[Diagnosis of liver function in children using 131-I BSP]G Kirsch, V Pink, H Reddemann, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Use of a fluorogenic substrate, 6-hexadecanoylamino-4-methylumbelliferyl-beta-D-galactopyranoside, in the diagnosis of Krabbe diseaseU Grimm, M Zschiesche, G Widerschain, et al.
Human Genetics|January 1, 1983
Reliability of the Tønnesen technique for the identification of Hunter carriersL Petruschka, G Machill, M Wehnert, et al.
Biomedica Biochimica Acta|January 1, 1990
Tryptophan metabolic studies in patients with presenile cataractsU Grimm, A Knapp, G Seidlitz, et al.
Zeitschrift Fur Arztliche Fortbildung|January 1, 1988
[Genetic diagnosis in classical phenylketonuria]K Wulff, F H Herrmann, M Wehnert, et al.
Prenatal Diagnosis|June 1, 1989
Prenatal diagnosis of phenylketonuria by haplotype analysisK Wulff, M Wehnert, M Schütz, et al.
Clinical Genetics|September 1, 1988
Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic RepublicF H Herrmann, K Wulff, M Wehnert, et al.
Human Mutation|January 1, 1994
Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II)W Schröder, K Wulff, M Wehnert, et al.
Biomedica Biochimica Acta|January 1, 1983
[Detection of phenylalanine hydroxylase activity in leukocytes and fibroblasts]U Grimm, A Knapp, A Weber, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Zeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|July 1, 1983
[Homocystinuria]G Müller, H Lubs, G Seidlitz, et al.
Radiobiologia, Radiotherapia|January 1, 1976
[Diagnosis of liver function in children using 131-I BSP]G Kirsch, V Pink, H Reddemann, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Use of a fluorogenic substrate, 6-hexadecanoylamino-4-methylumbelliferyl-beta-D-galactopyranoside, in the diagnosis of Krabbe diseaseU Grimm, M Zschiesche, G Widerschain, et al.
Human Genetics|January 1, 1983
Reliability of the Tønnesen technique for the identification of Hunter carriersL Petruschka, G Machill, M Wehnert, et al.
Biomedica Biochimica Acta|January 1, 1990
Tryptophan metabolic studies in patients with presenile cataractsU Grimm, A Knapp, G Seidlitz, et al.
Zeitschrift Fur Arztliche Fortbildung|January 1, 1988
[Genetic diagnosis in classical phenylketonuria]K Wulff, F H Herrmann, M Wehnert, et al.
Prenatal Diagnosis|June 1, 1989
Prenatal diagnosis of phenylketonuria by haplotype analysisK Wulff, M Wehnert, M Schütz, et al.
Clinical Genetics|September 1, 1988
Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic RepublicF H Herrmann, K Wulff, M Wehnert, et al.
Human Mutation|January 1, 1994
Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II)W Schröder, K Wulff, M Wehnert, et al.
Biomedica Biochimica Acta|January 1, 1983
[Detection of phenylalanine hydroxylase activity in leukocytes and fibroblasts]U Grimm, A Knapp, A Weber, et al.
Pageof 5