Klaus Bender
Affiliations: | Human genetics and Anthropology | Albert-Ludwigs-University Freiburg, Freiburg im Breisgau, Baden-Württemberg, Germany |
Area:
Human geneticsGoogle:
"Klaus Bender"Cross-listing: GenetiTree
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Bender K, Beller G, Lautsch S. (1998) Tetranucleotide short tandem repeat polymorphisms and their possible mode of origin Cytogenetics and Cell Genetics. 80: 34-36 |
Otsen M, Den Bieman M, Winer ES, et al. (1995) Use of simple sequence length polymorphisms for genetic characterization of rat inbred strains. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 595-601 |
Bender K, Seibert RT, Wienker TF, et al. (1994) Biochemical genetics of methylglyoxal dehydrogenases in the laboratory rat (Rattus norvegicus) Biochemical Genetics. 32: 147-154 |
Bender K, Kasulke D, Mayerova A, et al. (1991) New mutation versus exclusion at the alpha-1-antitrypsin locus: A multifaceted approach in a problematical paternity case Human Heredity. 41: 1-11 |
Koch MC, Ricker K, Otto M, et al. (1991) Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17. Journal of Medical Genetics. 28: 583-6 |
Koch MC, Ricker K, Otto M, et al. (1991) Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17. Human Genetics. 88: 71-4 |
Bender K, Senff H, Wienker TF, et al. (1990) A linkage study of malignant hyperthermia (MH) Clinical Genetics. 37: 221-225 |
Steuer M, Mauff G, Adam C, et al. (1989) An estimate on the frequency of duplicated haplotypes and silent alleles of human C4 protein polymorphism. I. Investigations in healthy Caucasoid families Tissue Antigens. 33: 501-510 |
Geserick G, Mauff G, Siemens I, et al. (1989) Human BF*F-subtypes: segregation analysis with inclusion of MHC haplotypes Human Genetics. 83: 252-256 |
Koch M, Harley H, Sarfarazi M, et al. (1989) Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19 Human Genetics. 82: 163-166 |