Bernd Dworniczak

Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens

Thilo Dörk, Bernd Dworniczak, C. Aulehla‐Scholz et al. · Human Genetics · 1997 · 256 citations

Developmental Anomaly, Distinct Spectrum, Developmental Biology +11

A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome

Barbara L�decke, Bernd Dworniczak, K. Bartholom� · Human Genetics · 1995 · 204 citations

Tyrosine Hydroxylase Gene, Developmental Biology, Mendelian Disorder +9

Immunosuppression and Renal Outcome in Congenital and Pediatric Steroid-Resistant Nephrotic Syndrome

Anja Büscher, Birgitta Kranz, Rainer Büscher et al. · Clinical Journal of the American Society of Nephrology · 2010 · 180 citations · Full text

RNA polymerase II of Drosophila

Dieter Falkenburg, Bernd Dworniczak, Daniela M. Faust et al. · Journal of Molecular Biology · 1987 · 114 citations

Rna Polymerase Ii, Natural Sciences, Genetics +6

New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia

Sergio Laínez, Karl P. Schlingmann, Jenny van der Wijst et al. · European Journal of Human Genetics · 2013 · 89 citations · Full text

Genetic Disorder, Genetics, Molecular Biology +4