APA

Kleefstra T., van Zelst-Stams W. A., Nillesen W. M., Cormier-Daire V., Houge G., Foulds N., van Dooren M., Willemsen M. H., Pfundt R., Turner A., Wilson M., McGaughran J., Rauch A., Zenker M., Adam M. P., Innes M., Davies C., López A. G., Casalone R., Weber A., Brueton L. A., Navarro A. D., Bralo M. P., Venselaar H., Stegmann S. P. A., Yntema H. G., van Bokhoven H. & Brunner H. G. (20091231). Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype. : Journal of medical genetics.

Chicago

Kleefstra T, van Zelst-Stams W A, Nillesen W M, Cormier-Daire V, Houge G, Foulds N, van Dooren M, Willemsen M H, Pfundt R, Turner A, Wilson M, McGaughran J, Rauch A, Zenker M, Adam M P, Innes M, Davies C, López A González-Meneses, Casalone R, Weber A, Brueton L A, Navarro A Delicado, Bralo M Palomares, Venselaar H, Stegmann S P A, Yntema H G, van Bokhoven H and Brunner H G. 20091231. Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype. : Journal of medical genetics.

Harvard

Kleefstra T., van Zelst-Stams W. A., Nillesen W. M., Cormier-Daire V., Houge G., Foulds N., van Dooren M., Willemsen M. H., Pfundt R., Turner A., Wilson M., McGaughran J., Rauch A., Zenker M., Adam M. P., Innes M., Davies C., López A. G., Casalone R., Weber A., Brueton L. A., Navarro A. D., Bralo M. P., Venselaar H., Stegmann S. P. A., Yntema H. G., van Bokhoven H. and Brunner H. G. (20091231). Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype. : Journal of medical genetics.

MLA

Kleefstra T, van Zelst-Stams W A, Nillesen W M, Cormier-Daire V, Houge G, Foulds N, van Dooren M, Willemsen M H, Pfundt R, Turner A, Wilson M, McGaughran J, Rauch A, Zenker M, Adam M P, Innes M, Davies C, López A González-Meneses, Casalone R, Weber A, Brueton L A, Navarro A Delicado, Bralo M Palomares, Venselaar H, Stegmann S P A, Yntema H G, van Bokhoven H and Brunner H G. Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype. : Journal of medical genetics. 20091231.