Fokstuen, S. Et Al. 1998. 22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin. CLINICAL GENETICS , vol.53, no.1 , 63-69.

Fokstuen, S., Arbenz, U., Artan, S., Dutly, F., Bauersfeld, U., Brecevic, L., ... Fasnacht, M.(1998). 22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin. CLINICAL GENETICS , vol.53, no.1, 63-69.

Fokstuen, S Et Al. "22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin," CLINICAL GENETICS , vol.53, no.1, 63-69, 1998

Fokstuen, S Et Al. "22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin." CLINICAL GENETICS , vol.53, no.1, pp.63-69, 1998

Fokstuen, S. Et Al. (1998) . "22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin." CLINICAL GENETICS , vol.53, no.1, pp.63-69.

@article{article, author={S Fokstuen Et Al. }, title={22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin}, journal={CLINICAL GENETICS}, year=1998, pages={63-69} }