Dibbens, L. M. Et Al. 2009. Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. HUMAN MOLECULAR GENETICS , vol.18, no.19 , 3626-3631.

Dibbens, L. M., Mullen, S., Helbig, I., Mefford, H. C., Bayly, M. A., Bellows, S., ... Leu, C.(2009). Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. HUMAN MOLECULAR GENETICS , vol.18, no.19, 3626-3631.

Dibbens, Leanne Et Al. "Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance," HUMAN MOLECULAR GENETICS , vol.18, no.19, 3626-3631, 2009

Dibbens, Leanne M. Et Al. "Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance." HUMAN MOLECULAR GENETICS , vol.18, no.19, pp.3626-3631, 2009

Dibbens, L. M. Et Al. (2009) . "Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance." HUMAN MOLECULAR GENETICS , vol.18, no.19, pp.3626-3631.

@article{article, author={Leanne M. Dibbens Et Al. }, title={Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance}, journal={HUMAN MOLECULAR GENETICS}, year=2009, pages={3626-3631} }