J. Schmidtke

Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene

Lucy R. Osborne, George Santis, Martin Schwarz et al. · Human Genetics · 1992 · 79 citations

Fibrosis, Mendelian Disorder, Genetic Disorder +9

Evolutionary conservation of a common pattern of activity of nucleolus organizers during spermatogenesis in vertebrates

Michael Schmid, C. L�ser, J. Schmidtke et al. · Chromosoma · 1982 · 78 citations

Spermatogenesis, Fertility, Reproductive Biology +16

Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families

Michael Krawczak, David Konecki, J. Schmidtke et al. · Human Genetics · 1988 · 65 citations

Dna Markers, Allelic Variant, Allelic Association +12

Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21‐q23

Manfred Stuhrmann, HC Hennies, Kai Brakensiek et al. · Clinical Genetics · 2008 · 62 citations

Novel and characteristic CFTR mutations in Saudi Arab children with severe cystic fibrosis.

E.A. El-Harith, Thilo Dörk, Manfred Stuhrmann et al. · Journal of Medical Genetics · 1997 · 58 citations · Full text