Roessler, E., Ma, Y., Ouspenskaia, M. V., Lacbawan, F., Bendavid, C., Dubourg, C., . . . Muenke, M. (2009). Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans.

Roessler, Erich, Yong Ma, Maia V. Ouspenskaia, Felicitas Lacbawan, Claude Bendavid, Christèle Dubourg, Philip A. Beachy, and Maximilian Muenke. Truncating Loss-of-function Mutations of DISP1 Contribute to Holoprosencephaly-like Microform Features in Humans. 2009.

Roessler, Erich, et al. Truncating Loss-of-function Mutations of DISP1 Contribute to Holoprosencephaly-like Microform Features in Humans. 2009.