Stoilov, I. Et Al. 1997. Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21. HUMAN MOLECULAR GENETICS , vol.6, no.4 , 641-647.

Stoilov, I., Akarsu, A. N., & Sarfarazi, M., (1997). Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21. HUMAN MOLECULAR GENETICS , vol.6, no.4, 641-647.

Stoilov, I, AYŞE NURTEN AKARSU, And M Sarfarazi. "Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21," HUMAN MOLECULAR GENETICS , vol.6, no.4, 641-647, 1997

Stoilov, I Et Al. "Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21." HUMAN MOLECULAR GENETICS , vol.6, no.4, pp.641-647, 1997

Stoilov, I. Akarsu, A. N. And Sarfarazi, M. (1997) . "Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21." HUMAN MOLECULAR GENETICS , vol.6, no.4, pp.641-647.

@article{article, author={I Stoilov Et Al. }, title={Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21}, journal={HUMAN MOLECULAR GENETICS}, year=1997, pages={641-647} }