H. Benkmann

发表

Polymorphism of delta-aminolevulinic acid dehydratase in lead-exposed workers

J. Angerer, H. Goedde, G. Lehnert, 1986, International archives of occupational and environmental health.

Distribution of alpha-1-antitrypsin and haptoglobin phenotypes in bladder cancer patients.

H. Hanssen, H. Goedde, R. Ovenbeck, 1987, Human heredity.

Levels of serum β1c/β1A globulin (C3) and its polymorphism in leprosy patients and healthy controls from Ethiopia and Mali

H. Delbrück, D. Agarwal, H. Goedde, 1974, Humangenetik.

Studies on the polymorphism of C3, Tf and Bg in Down's syndrome and other diseases

L. M. Srivastava, D. Agarwal, H. Goedde, 1975, Humangenetik.

Aldehyde dehydrogenase isozyme deficiency and alcohol sensitivity in four different Chinese populations.

Jiujin Xu, P. Bogdański, D. Agarwal, 1984, Human Heredity.

Studies of amniotic fluid and cord blood in an infant with alpha1-antitrypsin deficiency

D. Kaiser, P. Kehrli, O. Rennert, 2004, Humangenetik.

Ecogenetic and Pharmacogenetic Phenomena

H. Goedde, H. Benkmann, 1991 .

Genetic studies in Atacameño Indians: serum protein and red cell-enzyme polymorphisms.

F. Rothhammer, P. Bogdański, H. Goedde, 1985, Annals of human biology.

Studies on the change of electrophoretic mobility and the decay of catalytic activity of brain-type creatine kinase isoenzyme (CK-BB) following incubation at 37 degrees C.

J. Hoo, H. Goedde, H. Benkmann, 1981, Clinica chimica acta; international journal of clinical chemistry.

Population genetic studies of serum protein polymorphisms in four Spanish populations. II.

H. Goedde, Á. Pellicer, H. Benkmann, 1973, Human heredity.

Creatine kinase * isoenzyme patterns in Duchenne muscular dystrophy

H. Goedde, H. Lang, H. Benkmann, 1978, Clinical genetics.

Genetic studies in Ecuador: acetylator phenotypes, red cell enzyme and serum protein polymorphisms of Shuara Indians.

D. Agarwal, H. Goedde, H. Benkmann, 1977, American journal of physical anthropology.

Monomorphism of formaldehyde dehydrogenase in different populations.

D. Agarwal, N. Saha, H. Goedde, 1991, Human heredity.

Genetic studies in Saudi Arabia: red cell enzyme, haemoglobin and serum protein polymorphisms.

M. Dietrich, E. Kohne, D. Agarwal, 1979, American journal of physical anthropology.

Genetic polymorphism of C3 and serum levels of immunoglobulins, C3, C4 components of complement and C3-proactivator in four different populations of Afghanistan

H. Delbrück, D. Agarwal, G. Flatz, 1976, Human Genetics.

Genetic Markers, Serum Protein and Erythrocyte Enzyme Polymorphisms

H. Goedde, H. Benkmann, 1991 .

The use of serum cholinesterase in succinylcholine apnoea

H. Goedde, H. Benkmann, K. Scholler, 1977, Canadian Anaesthetists' Society journal.

Hereditary ataxia and the sixth chromosome.

A. Koeppen, H. Goedde, H. Benkmann, 1981, Archives of neurology.

Population genetic studies in three Chinese minorities.

P. Bogdański, L. Z. Chen, H. Goedde, 1984, American journal of physical anthropology.

Polymorphisms of Pi, Hp, ADA and AK in Mongolian, Korean and Zhuang populations of China.

P. Bogdański, L. Z. Chen, H. Goedde, 1986, Annals of human biology.

Distribution of eight blood-group systems and ABH secretion in Mongolian, Korean, and Zhuang nationalities in China.

L. Z. Chen, H. Goedde, H. Benkmann, 1984, Annals of human biology.

Isoelectric focusing studies of human red cell PGM1 in Japanese, with special reference to the characterization of PGM17.

H. Goedde, H. Benkmann, I. Nishigaki, 1982, Human heredity.

Red cell enzyme polymorphisms in different populations of Afghanistan.

H. Delbrück, G. Flatz, H. Goedde, 1977, Annals of human biology.

Properdin factor B polymorphism in Afghanistan.

H. Delbrück, D. Agarwal, G. Flatz, 1980, Human heredity.

Genetic studies in Cameroon: red cell enzyme and serum protein polymorphisms.

D. Agarwal, B. Brinkmann, U. Bienzle, 1979, Zeitschrift fur Morphologie und Anthropologie.

Phylogenetic resolution of complex mutational features at Y-STR DYS390 in aboriginal Australians and Papuans.

P. Forster, L. Roewer, M. Kayser, 1998, Molecular biology and evolution.

Genetic survey in the population of Assam. II. Serum protein and erythrocyte enzyme polymorphisms.

H. Delbrück, M. R. Chakravartti, G. Flatz, 1972, Human heredity.

Population genetic studies of red cell enzyme polymorphisms in four Spansih populations.

H. Goedde, Á. Pellicer, H. Benkmann, 1972, Human heredity.

Gene frequencies of red cell adenosine deaminase, adenylate kinase, phosphoglucomutase, acid phosphatase and serum α1-antitrypsin (Pi) in a German population

H. Goedde, H. Benkmann, Surjit Singh, 2004, Humangenetik.

Family studies on the third component of complement (C3), 6h1-antitrypsin polymorphism (locus E1 and E2) in the area of Marburg (Germany)

H. Goedde, H. Benkmann, G. Wendt, 2005, Humangenetik.

Adenylate kinase polymorphism in populations in Finland (Swedes, Finns, Lapps), in Maris, and in Greenland Eskimos

A. Eriksson, J. Fellman, H. Goedde, 2004, Humangenetik.

Genetic polymorphism of C′3 (β1C-globulin) component of complement in a German and a Spanish population

H. Goedde, H. Benkmann, L. Hirth, 2004, Humangenetik.

Polymorphism of delta-aminolevulinic acid dehydratase in various populations.

P. Bogdański, H. Goedde, H. Benkmann, 1983, Human heredity.

Ecogenetic studies in Atacameño Indians

F. Rothhammer, P. Bogdański, H. Goedde, 2004, Human Genetics.

The acetylator polymorphism in four populations of Afghanistan.

H. Delbrück, G. Flatz, H. Goedde, 1977, Human heredity.

Ultrathin-layer isoelectrofocusing for rapid diagnosis of protein variants

H. Goedde, H. Benkmann, L. Hirth, 2004, Human Genetics.

Serum protein polymorphisms in four populations of Afghanistan.

H. Delbrück, G. Flatz, H. Goedde, 1977, American journal of human genetics.

Genetic studies in Egypt: red cell enzyme and plasma protein polymorphisms.

H. Goedde, H. Benkmann, L. Hussein, 1980, Zeitschrift fur Morphologie und Anthropologie.

Red cell enzyme and serum protein polymorphisms in South Korea.

I. K. Kim, Y. Paik, H. Goedde, 1989, Human heredity.

Drinking Behaviour and Alcoholism

H. Goedde, H. Benkmann, A. Czeizel, 1991 .

Activity of creatine kinase isoenzyme MB in serum and red cell acetylcholinesterase variants in patients with duchenne muscular dystrophy

D. Agarwal, H. Goedde, H. Lang, 1977, Klinische Wochenschrift.

δ‐aminolevulinic acid dehydrase (porphobilinogen synthase) in two families with inherited enzyme deficiency

M. Doss, H. Goedde, H. Benkmann, 1986, Clinical genetics.

Red cell and serum protein polymorphisms in three population groups of South Korea.

P. Bogdański, Y. Paik, H. Goedde, 1987, Gene geography : a computerized bulletin on human gene frequencies.

Genetics of the Hungarian Population

A. Czeizel, H. Goedde, H. Benkmann, 1991 .

Distribution of apolipoprotein E genotypes in Asian Indians, Hungarians, and Papua New Guineans.

L. M. Srivastava, D. Agarwal, H. Goedde, 1996, Anthropologischer Anzeiger; Bericht uber die biologisch-anthropologische Literatur.

Further Investigations on the Inherited Polymorphism of the Third Component of Complement (β1C/β1A-Globulin)

D. Agarwal, H. Goedde, H. Benkmann, 1972 .

Family studies on the third component of complement (C3), 1-antitrypsin and pseudocholinesterase polymorphism (locus E 1 and E 2 ) in the area of Marburg (Germany).

H. Goedde, H. Benkmann, G. Wendt, 1972, Humangenetik.

Genetic polymorphism of the third component of complement (C3) and levels of 1 C- 1 A-globulin in sera of German and Spanish populations.

D. Agarwal, H. Goedde, H. Benkmann, 1972, Human heredity.

GENETIC LINKAGE IN HEREDITARY ATAXIA

A. Koeppen, H. Goedde, H. Benkmann, 1980, The Lancet.

Linkage Studies between HL‐A and GPT Polymorphisms and Other Genetic Markers 1

H. Hoppe, K. Saternus, H. Goedde, 1976, Vox sanguinis.

alpha1-Antitrypsin-Mangel im Säuglingsalter

V. Totović, H. Rotthauwe, J. Sennekamp, 1975 .

[Malignant hyperthermia during the 13th general anaesthesia (author's transl)].

K. Püschel, B. Brinkmann, H. Benkmann, 1978, Der Anaesthesist.