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G Machill

Showing results (31-40 of 41) 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.
Zentralblatt Fur Gynakologie|January 1, 1975
[Prenatal brain damage in maternal, untreated phenylketonuria]W H Peters, H Lubs, G Machill, et al.
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik|January 1, 1988
[Modified treatment of DNA preparation for cultured amniotic fluid cells and chorionic tissue]M Wehnert, U Kiessling, M Schütz, et al.
Zeitschrift Fur Arztliche Fortbildung|January 1, 1988
[Phenylketonuria from the current viewpoint]G Seidlitz, G Machill, U Grimm, et al.
Human Heredity|January 1, 1991
Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C geneM Wehnert, G Machill, T Grimm, et al.
Das Deutsche Gesundheitswesen|October 14, 1971
[Routine early diagnosis of phenylketonuria using the Guthrie test in the GDR]G Machill, K Schlenzka, G Cobet, 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.
Ceskoslovenska Pediatrie|May 1, 1985
[Metachromatic leukodystrophy with a familial incidence; prenatal diagnosis]A Pijácková, Z Kaláb, G Machill, et al.
Acta Biologica Et Medica Germanica|January 1, 1975
[Determination of kynureninase activity in oligophrenic children with hereditary taint, before and after vitamin B6 treatment]U Grimm, A Knapp, G Machill, et al.
European Journal of Pediatrics|January 1, 1994
Results of selective screening for inborn errors of metabolism in the former East GermanyG Machill, U Grimm, I Ahlbehrendt, et al.
Pageof 5

Showing results (31-40 of 41) 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.
Zentralblatt Fur Gynakologie|January 1, 1975
[Prenatal brain damage in maternal, untreated phenylketonuria]W H Peters, H Lubs, G Machill, et al.
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik|January 1, 1988
[Modified treatment of DNA preparation for cultured amniotic fluid cells and chorionic tissue]M Wehnert, U Kiessling, M Schütz, et al.
Zeitschrift Fur Arztliche Fortbildung|January 1, 1988
[Phenylketonuria from the current viewpoint]G Seidlitz, G Machill, U Grimm, et al.
Human Heredity|January 1, 1991
Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C geneM Wehnert, G Machill, T Grimm, et al.
Das Deutsche Gesundheitswesen|October 14, 1971
[Routine early diagnosis of phenylketonuria using the Guthrie test in the GDR]G Machill, K Schlenzka, G Cobet, 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.
Ceskoslovenska Pediatrie|May 1, 1985
[Metachromatic leukodystrophy with a familial incidence; prenatal diagnosis]A Pijácková, Z Kaláb, G Machill, et al.
Acta Biologica Et Medica Germanica|January 1, 1975
[Determination of kynureninase activity in oligophrenic children with hereditary taint, before and after vitamin B6 treatment]U Grimm, A Knapp, G Machill, et al.
European Journal of Pediatrics|January 1, 1994
Results of selective screening for inborn errors of metabolism in the former East GermanyG Machill, U Grimm, I Ahlbehrendt, et al.
Pageof 5