A Second Locus ( GLC3B ) for Primary Congenital Glaucoma (Buphthalmos) Maps to the 1p36 Region

By Akarsu A. Nurten   Turacli M. Erol   Aktan S. Gulderen   Barsoum-Homsy Magda   Chevrette Line   Sayli B. Sitki   Sarfarazi Mansoor  

Human Molecular Genetics, Vol. 5, Iss. 8, 1996-01 ,pp. : 1199-1203

Oxford University Press

Access to resources Recommend Favorite

Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus

By Bejjani Bassem A.  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 367-374

Oxford University Press

Access to resources Recommend Favorite

A polymorphism in the CYP1B1 promoter is functionally associated with primary congenital glaucoma

By Chakrabarti Subhabrata   Ghanekar Yashoda   Kaur Kiranpreet   Kaur Inderjeet   Mandal Anil K.   Rao Kollu N.   Parikh Rajul S.   Thomas Ravi   Majumder Partha P.  

Human Molecular Genetics, Vol. 19, Iss. 20, 2010-10 ,pp. : 4083-4090

Oxford University Press

Access to resources Recommend Favorite

Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions

By  

Molecular Syndromology, Vol. 5, Iss. 2, 2014-01 ,pp. : 57-64

Karger

Access to resources Recommend Favorite

Cytochrome P4501A1, glutathione S-transferase M1 and T1 gene polymorphisms in chronic myeloid leukemia

By Ovsepyan V.   Vinogradova E.   Sherstneva E.  

Russian Journal of Genetics, Vol. 46, Iss. 10, 2010-10 ,pp. : 1201-1202

MAIK Nauka/Interperiodica

Access to resources Recommend Favorite