APA

Twigg S. R. F., Versnel S. L., Nürnberg G., Lees M. M., Bhat M., Hammond P., Hennekam R. C. M., Hoogeboom A. J. M., Hurst J. A., Johnson D., Robinson A. A., Scambler P. J., Gerrelli D., Nürnberg P., Mathijssen I. M. J. & Wilkie A. O. M. (20090609). Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. : American journal of human genetics.

Chicago

Twigg Stephen R F, Versnel Sarah L, Nürnberg Gudrun, Lees Melissa M, Bhat Meenakshi, Hammond Peter, Hennekam Raoul C M, Hoogeboom A Jeannette M, Hurst Jane A, Johnson David, Robinson Alexis A, Scambler Peter J, Gerrelli Dianne, Nürnberg Peter, Mathijssen Irene M J and Wilkie Andrew O M. 20090609. Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. : American journal of human genetics.

Harvard

Twigg S. R. F., Versnel S. L., Nürnberg G., Lees M. M., Bhat M., Hammond P., Hennekam R. C. M., Hoogeboom A. J. M., Hurst J. A., Johnson D., Robinson A. A., Scambler P. J., Gerrelli D., Nürnberg P., Mathijssen I. M. J. and Wilkie A. O. M. (20090609). Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. : American journal of human genetics.

MLA

Twigg Stephen R F, Versnel Sarah L, Nürnberg Gudrun, Lees Melissa M, Bhat Meenakshi, Hammond Peter, Hennekam Raoul C M, Hoogeboom A Jeannette M, Hurst Jane A, Johnson David, Robinson Alexis A, Scambler Peter J, Gerrelli Dianne, Nürnberg Peter, Mathijssen Irene M J and Wilkie Andrew O M. Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. : American journal of human genetics. 20090609.