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Humangenetik
|
January 1, 1971
New biochemical and immunological data on quantitative and qualitative variability of human pseudocholinesterase
K Altland, H W Goedde, K Held, et al.
Archives of Neurology
|
March 1, 1981
Hereditary ataxia and the sixth chromosome
A H Koeppen, H W Goedde, C Hiller, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1986
A case of Lesch Nyhan syndrome with delayed onset of self-mutilation: search for abnormal biochemical, immunological and cell growth characteristic in fibroblasts and neurotransmitters in urine
S Singh, I Willers, K Ullrich, et al.
MMW, Munchener Medizinische Wochenschrift
|
July 13, 1979
[Perforating sigmoid diverticulitis in monozygotic twins]
H H Pusch, G Börger, L Hirth, et al.
Lancet (London, England)
|
January 12, 1980
Genetic linkage in hereditary ataxia
A H Koeppen, H W Goedde, L Hirth, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
"High Km" aldehyde dehydrogenase isozymes in human tissues: constitutive and tumor-associated forms
D P Agarwal, R Eckey, A C Rudnay, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry
|
August 1, 1992
Human liver glutamic gamma-semialdehyde dehydrogenase: structural relationship to the yeast enzyme
J Hempel, R Eckey, D Berie, et al.
Humangenetik
|
January 1, 1971
Pseudocholinesterase polymorphism among Lapp populations in Finland
S Singh, M Jensen, H W Goedde, et al.
Human Heredity
|
January 1, 1974
Phenotypes of Gc and Tf in leprosy patients of Mali and Ethiopia
H W Goedde, H G Benkmann, L Hirth, et al.
Human Genetics
|
January 1, 1981
A radioenzymatic assay of catechol-O-methyltransferase in hair root cells: comparison with erythrocyte activity
J J Hoo, T Strohmeyer, W J Beckermann, et al.
Page
of 27
Search research articles
Search
Showing results (201-210 of 269) with videos related to
Sort By:
Page
of 27
Humangenetik
|
January 1, 1971
New biochemical and immunological data on quantitative and qualitative variability of human pseudocholinesterase
K Altland, H W Goedde, K Held, et al.
Archives of Neurology
|
March 1, 1981
Hereditary ataxia and the sixth chromosome
A H Koeppen, H W Goedde, C Hiller, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1986
A case of Lesch Nyhan syndrome with delayed onset of self-mutilation: search for abnormal biochemical, immunological and cell growth characteristic in fibroblasts and neurotransmitters in urine
S Singh, I Willers, K Ullrich, et al.
MMW, Munchener Medizinische Wochenschrift
|
July 13, 1979
[Perforating sigmoid diverticulitis in monozygotic twins]
H H Pusch, G Börger, L Hirth, et al.
Lancet (London, England)
|
January 12, 1980
Genetic linkage in hereditary ataxia
A H Koeppen, H W Goedde, L Hirth, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
"High Km" aldehyde dehydrogenase isozymes in human tissues: constitutive and tumor-associated forms
D P Agarwal, R Eckey, A C Rudnay, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry
|
August 1, 1992
Human liver glutamic gamma-semialdehyde dehydrogenase: structural relationship to the yeast enzyme
J Hempel, R Eckey, D Berie, et al.
Humangenetik
|
January 1, 1971
Pseudocholinesterase polymorphism among Lapp populations in Finland
S Singh, M Jensen, H W Goedde, et al.
Human Heredity
|
January 1, 1974
Phenotypes of Gc and Tf in leprosy patients of Mali and Ethiopia
H W Goedde, H G Benkmann, L Hirth, et al.
Human Genetics
|
January 1, 1981
A radioenzymatic assay of catechol-O-methyltransferase in hair root cells: comparison with erythrocyte activity
J J Hoo, T Strohmeyer, W J Beckermann, et al.
Page
of 27