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G Machill

Showing results (21-30 of 41) with videos related to

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Acta Biologica Et Medica Germanica|January 1, 1972
[Immune reactions of rats with experimental induced hyperphenylalaninemia]U Haufe, F Haufe, H Lubs, 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.
Kinderarztliche Praxis|October 1, 1986
[Current aspects of mucoviscidosis screening in East Germany]J Hein, H J Dietzsch, G Machill, et al.
Ceskoslovenska Pediatrie|November 1, 1973
[Results of screening and early treatment of phenylketonuria in the GDR (German Democratic Republic)]G Machill, K Schlenzka, L Landstätter, et al.
Acta Biologica Et Medica Germanica|January 1, 1975
[Alpha-L-iduronidase activity in fibroblasts of patients with Hurler syndrome]G Stareprawo, U Grimm, G Machill, et al.
Ceskoslovenska Pediatrie|June 1, 1984
[Lesch-Nyhan syndrome]J Pajerek, J Kofer, Z Kulenda, et al.
Journal of Medical Genetics|June 1, 1991
Segregation and sporadic cases in families with Hunter's syndromeG Machill, G Barbujani, G A Danieli, et al.
Dermatologische Monatschrift|January 1, 1988
[Prenatal diagnosis of X chromosome recessive ichthyosis in uncultured chorion cells]U Grimm, F H Herrmann, G Machill, et al.
Acta Biologica Et Medica Germanica|January 1, 1974
[Simple microlitre-method for the determination of hypoxanthine-guanine-phosphoribosyl transferase activity in erythrocytes and skin fibroblasts]U Grimm, H Lubs, G Machill, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Acta Biologica Et Medica Germanica|January 1, 1972
[Immune reactions of rats with experimental induced hyperphenylalaninemia]U Haufe, F Haufe, H Lubs, 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.
Kinderarztliche Praxis|October 1, 1986
[Current aspects of mucoviscidosis screening in East Germany]J Hein, H J Dietzsch, G Machill, et al.
Ceskoslovenska Pediatrie|November 1, 1973
[Results of screening and early treatment of phenylketonuria in the GDR (German Democratic Republic)]G Machill, K Schlenzka, L Landstätter, et al.
Acta Biologica Et Medica Germanica|January 1, 1975
[Alpha-L-iduronidase activity in fibroblasts of patients with Hurler syndrome]G Stareprawo, U Grimm, G Machill, et al.
Ceskoslovenska Pediatrie|June 1, 1984
[Lesch-Nyhan syndrome]J Pajerek, J Kofer, Z Kulenda, et al.
Journal of Medical Genetics|June 1, 1991
Segregation and sporadic cases in families with Hunter's syndromeG Machill, G Barbujani, G A Danieli, et al.
Dermatologische Monatschrift|January 1, 1988
[Prenatal diagnosis of X chromosome recessive ichthyosis in uncultured chorion cells]U Grimm, F H Herrmann, G Machill, et al.
Acta Biologica Et Medica Germanica|January 1, 1974
[Simple microlitre-method for the determination of hypoxanthine-guanine-phosphoribosyl transferase activity in erythrocytes and skin fibroblasts]U Grimm, H Lubs, G Machill, et al.
Pageof 5