F. Brancati Et Al. , "CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders," AMERICAN JOURNAL OF HUMAN GENETICS , vol.81, no.1, pp.104-113, 2007
Brancati, F. Et Al. 2007. CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. AMERICAN JOURNAL OF HUMAN GENETICS , vol.81, no.1 , 104-113.
Brancati, F., Barrano, G., Silhavy, J. L., Marsh, S. E., Travaglini, L., Bielas, S. L., ... Amorini, M.(2007). CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. AMERICAN JOURNAL OF HUMAN GENETICS , vol.81, no.1, 104-113.
Brancati, Francesco Et Al. "CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders," AMERICAN JOURNAL OF HUMAN GENETICS , vol.81, no.1, 104-113, 2007
Brancati, Francesco Et Al. "CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders." AMERICAN JOURNAL OF HUMAN GENETICS , vol.81, no.1, pp.104-113, 2007
Brancati, F. Et Al. (2007) . "CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders." AMERICAN JOURNAL OF HUMAN GENETICS , vol.81, no.1, pp.104-113.
@article{article, author={Francesco Brancati Et Al. }, title={CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2007, pages={104-113} }