686 results on '"Goedde, H. W."'
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2. Medicobiological and genetic studies on alcoholism Role of metabolic variation and ethnicity on drinking habits, alcohol abuse and alcohol-related mortality
3. Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?
4. Characterization of long-term cell cultures of human chorion villi and fibroblasts using antibodies to cytoskeletal proteins
5. Genetisch bedingte Variabilität des Alkoholstoffwechsels und ihr Einfluß auf Trinkverhalten und Neigung zum Alkoholismus
6. Drinking Behaviour and Alcoholism
7. Human variability in alcohol and aldehyde metabolism: vulnerability to toxic effects
8. Genetic Markers, Serum Protein and Erythrocyte Enzyme Polymorphisms
9. Topics, Materials and Methods
10. Conclusions
11. Ecogenetic and Pharmacogenetic Phenomena
12. Distribution of ADH2 and ALDH2 genotypes in different populations
13. Besonderheiten der Lippenfurchen bei den Eltern von Patienten mit Lippen-Kiefer-(Gaumen-)Spalten
14. Lippenfurchen und Hautleisten bei Zwillingen mit Lippen-Kiefer-(Gaumen-)Spalten
15. Papillarleisten der palmaren Interdigitalfelder — Aspekte bilateraler Asymmetrie
16. Supplementation and extension of the paper: "The distribution of human Gm-globulin and Inv-allotypes in populations of Egypt, Saudi-Arabia, Afghanistan and Ecuador"
17. Palmar epidermal ridges in lefthanders
18. Quantitative Parameter der digitalen Hautleisten — ihre Verteilung in Familien
19. Serum protein and erythrocyte enzyme polymorphisms in twelve population groups of Hungary
20. The Acetylator Polymorphism in four Populations of Afghanistan
21. Phenotypes of Gc and Tf in Leprosy Patients of Mali and Ethiopia
22. Pseudocholinesterase Polymorphism among Ålanders (Finno-Swedes), Maris (Cheremisses, USSR) and Greenland Eskimos, and the Segregation of some E₁ and E₂ Locus Types in Finnish Lapp Families
23. Properdin Factor B Polymorphism in Afghanistan
24. Purine Metabolism in Fibroblasts of Patients with Duchenne's Muscular Dystrophy
25. High HPRT Activity in Fibroblasts from Patients with Lesch-Nyhan Syndrome Due to Bacterial 'L-Form' Contamination
26. Nomenclature Of Pseudocholinesterase Polymorphism
27. Formalgenetische Untersuchungen über den Haptoglobin-Polymorphismus: Untersuchungen an 353 Familien
28. Studies on the Polymorphism of Isoniazid (INH) Acetylation in Rhesus Monkeys (Macaca Mulatta)
29. On Nomenclature of Pseudocholinesterase Polymorphism
30. Taste Thresholds of Thiourea Derivatives and Anetholtrithion in Twins
31. Untersuchungen der Hautfurchen bei Patienten mit endogenem Ekzem mit einem Beitrag zur Technik der Daktyloskopie
32. Über einige Serumproteinvarianten bei Primaten
33. Über erste Erfahrungen in der Anwendung des Pseudocholinesterase-Polymorphismus bei der Paternitätsbegutachtung
34. A Study of the Pseudocholinesterase Polymorphism Among a Panjabi Population
35. Red Cell Phosphoglucomutase Polymorphism in Finland-Swedes, Finns, Finnish Lapps, Maris (Cheremisses) and Greenland Eskimos, and Segregation Studies of PGM₁ Types in Lapp Families
36. Further Results on the Polymorphism of Soluble Glutamic-Pyruvic Transaminase (GPT; EC: 2.6.1.2) in a Population of Northern Germany
37. Genetic Survey in the Population of Assam: II. Serum Protein and Erythrocyte Enzyme Polymorphisms
38. Population Genetic Studies of Red Cell Enzyme Polymorphisms in Four Spanish Populations
39. Genetic Polymorphism of the Third Component of Complement (C3) and Levels of β₁C/β₁A-Globulin in Sera of German and Spanish Populations
40. Further Investigations on the Inherited Polymorphism of the Third Component of Complement (β₁C/β₁A-Globulin)
41. Population Genetic Studies of Serum Protein Polymorphisms in four Spanish Populations: Part II
42. A Note on Atypical Serum Cholinesterase and Genetic Factors in Leprosy
43. Genetic Polymorphism of C3: Levels of Total Hemolytic Complement Activity and β₁C-Globulin in Different Phenotypes of C3 in a North German Population
44. Klinik und Genetik der Pseudocholinesterasen
45. Arbeitsvorschriften : Nachweis, Identifizierung, Anreicherung und Auftrennung von normaler Pseudocholinesterase und Enzymvarianten sowie der Komponenten C1—C5
46. Biochemie und Genetik der Pseudocholinesterasen
47. PstI identifies biallelic DNA polymorphism of the human casein kinase 2α gene (CSNK2A1)
48. Two-dimensional electrophoresis of soluble and structure-bound proteins from cultured human fibroblasts and hair root cells: Qualitative and quantitative variation
49. Rapid determination of hypoxanthine-guanine-phosphoribosyl transferase in human fibroblasts and amniotic cells
50. Isozyme variations in acetaldehyde dehydrogenase (E.C.1.2.1.3) in human tissues
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