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G Seidlitz

Showing results (31-40 of 48) with videos related to

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Gynakologische Rundschau|January 1, 1989
[Genetic, biochemical and genomic prenatal diagnosis in genetic defects]G Göretzlehner, G Machill, U Grimm, et al.
European Journal of Pediatrics|July 1, 1996
German Maternal Phenylketonuria StudyS Cipcic-Schmidt, F K Trefz, B Fünders, et al.
Zeitschrift Fur Arztliche Fortbildung|January 1, 1988
[Phenylketonuria from the current viewpoint]G Seidlitz, G Machill, U Grimm, et al.
Zentralblatt Fur Allgemeine Pathologie U. Pathologische Anatomie|January 1, 1990
[Diagnosis of lysosomal storage diseases. Pathomorphologic and biochemical possibilities]C H August, H J Holzhausen, H Schmidt, et al.
Kinderarztliche Praxis|November 1, 1980
[Results and consequences of a social medical study in the region of Gera on Langdon-Down disease]M Kirchner, E Wolfram, U Pröhl, et al.
Zentralblatt Fur Gynakologie|January 1, 1988
[Diagnostic chorionic biopsies in the first trimester. Report of experiences over a 2 year period]M Schütz, W Knoll, D Grabow, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Mucopolysaccharidosis type II (Hunter syndrome): characterization of the iduronate-2-sulphatase in MPS II skin fibroblastsL Petruschka, M Zschiesche, J Bielicki, et al.
Journal of Medical Genetics|March 1, 1993
Carrier detection of Hunter syndrome (MPS II) by biochemical and DNA techniques in families at riskW Schröder, L Petruschka, M Wehnert, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
First prenatal diagnosis of acyl-CoA oxidase deficiencyR J Wanders, A Schelen, N Feller, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1992
[Maternal phenylketonuria. Problems in detecting and risk educating identified females]H J Salize, B Fünders-Bücker, U Knorrek, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Gynakologische Rundschau|January 1, 1989
[Genetic, biochemical and genomic prenatal diagnosis in genetic defects]G Göretzlehner, G Machill, U Grimm, et al.
European Journal of Pediatrics|July 1, 1996
German Maternal Phenylketonuria StudyS Cipcic-Schmidt, F K Trefz, B Fünders, et al.
Zeitschrift Fur Arztliche Fortbildung|January 1, 1988
[Phenylketonuria from the current viewpoint]G Seidlitz, G Machill, U Grimm, et al.
Zentralblatt Fur Allgemeine Pathologie U. Pathologische Anatomie|January 1, 1990
[Diagnosis of lysosomal storage diseases. Pathomorphologic and biochemical possibilities]C H August, H J Holzhausen, H Schmidt, et al.
Kinderarztliche Praxis|November 1, 1980
[Results and consequences of a social medical study in the region of Gera on Langdon-Down disease]M Kirchner, E Wolfram, U Pröhl, et al.
Zentralblatt Fur Gynakologie|January 1, 1988
[Diagnostic chorionic biopsies in the first trimester. Report of experiences over a 2 year period]M Schütz, W Knoll, D Grabow, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Mucopolysaccharidosis type II (Hunter syndrome): characterization of the iduronate-2-sulphatase in MPS II skin fibroblastsL Petruschka, M Zschiesche, J Bielicki, et al.
Journal of Medical Genetics|March 1, 1993
Carrier detection of Hunter syndrome (MPS II) by biochemical and DNA techniques in families at riskW Schröder, L Petruschka, M Wehnert, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
First prenatal diagnosis of acyl-CoA oxidase deficiencyR J Wanders, A Schelen, N Feller, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|January 1, 1992
[Maternal phenylketonuria. Problems in detecting and risk educating identified females]H J Salize, B Fünders-Bücker, U Knorrek, et al.
Pageof 5