Steven W. Scherer

Translocation breakpoint maps 5 kb 3 ′ from TWIST in a patient affected with Saethre–Chotzen syndrome (1997)

Inge Krebs, Isabel Weis, Melanie Hudler, Johanna M. Rommens, Helmut Roth, Steven W. Scherer, ...

Saethre–Chotzen syndrome, a common autosomal dominant craniosynostosis in humans, is characterized by brachydactyly, soft tissue syndactyly and facial dysmorphism including ptosis, facial...