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H Lubs

Showing results (11-20 of 47) with videos related to

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Neurofibromatosis|January 1, 1988
Variable expressivity of neurofibromatosis-1 in identical twinsM Bauer, H Lubs, M L Lubs
American Journal of Medical Genetics|January 1, 1984
A large kindred with X-linked mental retardation, marker X and macroorchidismH Lubs, H Travers, E Lujan, et al.
Laryngologie, Rhinologie, Otologie|September 1, 1974
[Screening test detection of genetic errors of metabolism in children with hearing defects (author's transl)]H Lubs, H Baumann, G Kluge, et al.
Acta Biologica Et Medica Germanica|January 1, 1971
[Behavior of serum amino acids in rats with experimentally produced hyperphenylalaninemia]H Lubs, G Machill, U Haufe, et al.
Zeitschrift Fur Urologie Und Nephrologie|December 1, 1988
[Distribution of cystinuria subtypes in the Democratic Republic of Germany]U Grimm, I Steinhauser, H Lubs, et al.
Acta Biologica Et Medica Germanica|January 1, 1971
[Kynureninase activity and pyridoxine elimination in rats with experimental phenylketonuria]G Machill, U Haufe, F Haufe, et al.
Acta Biologica Et Medica Germanica|January 1, 1972
[Immune reactions of rats with experimental induced hyperphenylalaninemia]U Haufe, F Haufe, H Lubs, et al.
Experimental and Clinical Endocrinology|August 1, 1988
The serum amino acid spectrum of insulin-dependent diabetics and controls from EthiopiaW H Peters, F T Lester, H Lubs
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik|January 1, 1983
[Homocystinuria - results of a screening test of risk groups and diagnosis of this genetic metabolic disorder]H Lubs, G Müller, G Seidlitz, et al.
Zeitschrift Fur Arztliche Fortbildung|July 15, 1981
[Mucopolysaccharidosis I in a pair of siblings]A Breninek, G Seidlitz, M Schaeper, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Neurofibromatosis|January 1, 1988
Variable expressivity of neurofibromatosis-1 in identical twinsM Bauer, H Lubs, M L Lubs
American Journal of Medical Genetics|January 1, 1984
A large kindred with X-linked mental retardation, marker X and macroorchidismH Lubs, H Travers, E Lujan, et al.
Laryngologie, Rhinologie, Otologie|September 1, 1974
[Screening test detection of genetic errors of metabolism in children with hearing defects (author's transl)]H Lubs, H Baumann, G Kluge, et al.
Acta Biologica Et Medica Germanica|January 1, 1971
[Behavior of serum amino acids in rats with experimentally produced hyperphenylalaninemia]H Lubs, G Machill, U Haufe, et al.
Zeitschrift Fur Urologie Und Nephrologie|December 1, 1988
[Distribution of cystinuria subtypes in the Democratic Republic of Germany]U Grimm, I Steinhauser, H Lubs, et al.
Acta Biologica Et Medica Germanica|January 1, 1971
[Kynureninase activity and pyridoxine elimination in rats with experimental phenylketonuria]G Machill, U Haufe, F Haufe, et al.
Acta Biologica Et Medica Germanica|January 1, 1972
[Immune reactions of rats with experimental induced hyperphenylalaninemia]U Haufe, F Haufe, H Lubs, et al.
Experimental and Clinical Endocrinology|August 1, 1988
The serum amino acid spectrum of insulin-dependent diabetics and controls from EthiopiaW H Peters, F T Lester, H Lubs
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik|January 1, 1983
[Homocystinuria - results of a screening test of risk groups and diagnosis of this genetic metabolic disorder]H Lubs, G Müller, G Seidlitz, et al.
Zeitschrift Fur Arztliche Fortbildung|July 15, 1981
[Mucopolysaccharidosis I in a pair of siblings]A Breninek, G Seidlitz, M Schaeper, et al.
Pageof 5