R. Hanke

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients

Uwe Lenk, R. Hanke, Hannelore Thiele et al. · Human Molecular Genetics · 1993 · 120 citations

Neurodegenerative Diseases, Rare Diseases, Dmd Patients +14

Relationship of polymorphisms in the renin-angiotensin system and in E-selectin of patients with early severe coronary heart disease

Katrin Wenzel, Anneke C. Blackburn, Monika Ernst et al. · Journal of Molecular Medicine · 1997 · 59 citations

Hypertension, Cardiovascular Disease, Genetic Epidemiology +10

Human X chromosome markers and Duchenne muscular dystrophy

Kay E. Davies, Andreas Speer, F. H. Herrmann et al. · Nucleic Acids Research · 1985 · 54 citations · Full text

Dna Markers, Cytogenetics, Genetics +18

Polymorphism in the human E-selectin gene detected by PCR-SSCP

Katrin Wenzel, R. Hanke, Astrid Speer · Human Genetics · 1994 · 42 citations

Genetics, Human Polymorphism, Immune-related Gene Polymorphism +2

Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy

Marco Sifringer, Birgit Uhlenberg, Stefanie Lammel et al. · Human Genetics · 2003 · 18 citations

Genetic Analysis, Functional Genomics, Subtraction Library +11