- 3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome. Willatt, L., Cox, J., Barber, J., Cabanas, E.D., Collins, A., Donnai, D., FitzPatrick, D.R., Maher, E., Martin, H., Parnau, J., Pindar, L., Ramsay, J., Shaw-Smith, C., Sistermans, E.A., Tettenborn, M., Trump, D., de Vries, B.B., Walker, K., Raymond, F.L. Am. J. Hum. Genet. (2005)