Sirmaci, A. Et Al. 2011. Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia. AMERICAN JOURNAL OF HUMAN GENETICS , vol.89, no.2 , 289-294.

Sirmaci, A., Spiliopoulos, M., Brancati, F., Powell, E., Duman, D., Abrams, A., ... Bademci, G.(2011). Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia. AMERICAN JOURNAL OF HUMAN GENETICS , vol.89, no.2, 289-294.

Sirmaci, Asli Et Al. "Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia," AMERICAN JOURNAL OF HUMAN GENETICS , vol.89, no.2, 289-294, 2011

Sirmaci, Asli Et Al. "Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia." AMERICAN JOURNAL OF HUMAN GENETICS , vol.89, no.2, pp.289-294, 2011

Sirmaci, A. Et Al. (2011) . "Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia." AMERICAN JOURNAL OF HUMAN GENETICS , vol.89, no.2, pp.289-294.

@article{article, author={Asli Sirmaci Et Al. }, title={Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2011, pages={289-294} }