W. Paznekas Et Al. , "Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia," AMERICAN JOURNAL OF HUMAN GENETICS , vol.72, no.2, pp.408-418, 2003
Paznekas, W. Et Al. 2003. Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia. AMERICAN JOURNAL OF HUMAN GENETICS , vol.72, no.2 , 408-418.
Paznekas, W., Boyadjiev, S., Shapiro, R., Daniels, O., Wollnik, B., Keegan, C., ... Innis, J.(2003). Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia. AMERICAN JOURNAL OF HUMAN GENETICS , vol.72, no.2, 408-418.
Paznekas, WA Et Al. "Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia," AMERICAN JOURNAL OF HUMAN GENETICS , vol.72, no.2, 408-418, 2003
Paznekas, WA Et Al. "Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia." AMERICAN JOURNAL OF HUMAN GENETICS , vol.72, no.2, pp.408-418, 2003
Paznekas, W. Et Al. (2003) . "Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia." AMERICAN JOURNAL OF HUMAN GENETICS , vol.72, no.2, pp.408-418.
@article{article, author={WA Paznekas Et Al. }, title={Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2003, pages={408-418} }