Joerg Schmidtke

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

T. Dörk, J. Schmidtke, M. Stuhrmann, 1997, Journal of medical genetics.

Prevalence of dural ectasia in 63 gene‐mutation‐positive patients with features of Marfan syndrome type 1 and Loeys‐Dietz syndrome and report of 22 novel FBN1 mutations

K. Rommel, J. Schmidtke, M. Arslan‐Kirchner, 2009, Clinical genetics.

A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis.

T. Meitinger, T. Dörk, K. Will, 1994, The Journal of clinical investigation.