CYP1B1 and primary congenital glaucoma: Chavarria-Soley G., Michels-Rautenstrauss K., Pasutto F., Flikier D.,Flikier P., Cirak S., Bejjani B., Winters D.L., Lewis R.A., Mardin C.,Reis A., Rautenstrauss B. Primary congenital glaucoma and Rieger’sanomaly: extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations.