Mitter, D., Schanze, D., Sterker, I., Müller, D., Till, H., & Zenker, M. (2012). MOTA Syndrome: Molecular Genetic Confirmation of the Diagnosis in a Newborn with Previously Unreported Clinical Features. S. Karger AG.

Mitter, D., D. Schanze, I. Sterker, D. Müller, H. Till, and M. Zenker. MOTA Syndrome: Molecular Genetic Confirmation of the Diagnosis in a Newborn With Previously Unreported Clinical Features. S. Karger AG, 2012.

Mitter, D., et al. MOTA Syndrome: Molecular Genetic Confirmation of the Diagnosis in a Newborn With Previously Unreported Clinical Features. S. Karger AG, 2012.