Kerstin Kutsche

Dural ectasia in Loeys–Dietz syndrome: comprehensive study of 30 patients with a TGFBR1 or TGFBR2 mutation

S. Blankenberg, K. Kutsche, B. Keyser, 2014, Clinical genetics.

Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation

S. Blankenberg, K. Kutsche, B. Keyser, 2014, Clinical genetics.

Neuro-kardio-fazio-kutane Syndrome

V. Mautner, M. Zenker, K. Kutsche, 2010 .