These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
243 related articles for article (PubMed ID: 21168818)
1. Genotype/phenotype correlation in primary congenital glaucoma patients from different ethnic groups of the Israeli population. Geyer O; Wolf A; Levinger E; Harari-Shacham A; Walton DS; Shochat C; Korem S; Bercovich D Am J Ophthalmol; 2011 Feb; 151(2):263-71.e1. PubMed ID: 21168818 [TBL] [Abstract][Full Text] [Related]
3. A clinical and molecular genetics study of primary congenital glaucoma in South Korea. Suh W; Kee C Br J Ophthalmol; 2012 Nov; 96(11):1372-7. PubMed ID: 22942166 [TBL] [Abstract][Full Text] [Related]
4. CYP1B1 gene analysis in primary congenital glaucoma Brazilian patients: novel mutations and association with poor prognosis. Della Paolera M; de Vasconcellos JP; Umbelino CC; Kasahara N; Rocha MN; Richeti F; Costa VP; Tavares A; de Melo MB J Glaucoma; 2010 Mar; 19(3):176-82. PubMed ID: 19528825 [TBL] [Abstract][Full Text] [Related]
5. A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG). El-Ashry MF; Abd El-Aziz MM; Bhattacharya SS J Glaucoma; 2007 Jan; 16(1):104-11. PubMed ID: 17224759 [TBL] [Abstract][Full Text] [Related]
6. Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients in the Lebanese Population: A Pilot Study. Al-Haddad C; Abdulaal M; Badra R; Barikian A; Noureddine B; Farra C Ophthalmic Genet; 2016; 37(1):31-6. PubMed ID: 24940937 [TBL] [Abstract][Full Text] [Related]
7. CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United States. Lim SH; Tran-Viet KN; Yanovitch TL; Freedman SF; Klemm T; Call W; Powell C; Ravichandran A; Metlapally R; Nading EB; Rozen S; Young TL Am J Ophthalmol; 2013 Mar; 155(3):508-517.e5. PubMed ID: 23218701 [TBL] [Abstract][Full Text] [Related]
8. Mutational screening of CYP1B1 in Turkish PCG families and functional analyses of newly detected mutations. Bagiyeva S; Marfany G; Gonzalez-Angulo O; Gonzalez-Duarte R Mol Vis; 2007 Aug; 13():1458-68. PubMed ID: 17893647 [TBL] [Abstract][Full Text] [Related]
9. CYP1B1 and MYOC Mutations in Vietnamese Primary Congenital Glaucoma Patients. Do T; Shei W; Chau PT; Trang DL; Yong VH; Ng XY; Chen YM; Aung T; Vithana EN J Glaucoma; 2016 May; 25(5):e491-8. PubMed ID: 26550974 [TBL] [Abstract][Full Text] [Related]
10. Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1. Hilal L; Boutayeb S; Serrou A; Refass-Buret L; Shisseh H; Bencherifa F; El Mzibri M; Benazzouz B; Berraho A Mol Vis; 2010 Jul; 16():1215-26. PubMed ID: 20664688 [TBL] [Abstract][Full Text] [Related]
11. Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene. Vincent AL; Billingsley G; Buys Y; Levin AV; Priston M; Trope G; Williams-Lyn D; Héon E Am J Hum Genet; 2002 Feb; 70(2):448-60. PubMed ID: 11774072 [TBL] [Abstract][Full Text] [Related]
12. Genotype and phenotype correlations in congenital glaucoma: CYP1B1 mutations, goniodysgenesis, and clinical characteristics. Hollander DA; Sarfarazi M; Stoilov I; Wood IS; Fredrick DR; Alvarado JA Am J Ophthalmol; 2006 Dec; 142(6):993-1004. PubMed ID: 17157584 [TBL] [Abstract][Full Text] [Related]
13. Myocilin gene implicated in primary congenital glaucoma. Kaur K; Reddy AB; Mukhopadhyay A; Mandal AK; Hasnain SE; Ray K; Thomas R; Balasubramanian D; Chakrabarti S Clin Genet; 2005 Apr; 67(4):335-40. PubMed ID: 15733270 [TBL] [Abstract][Full Text] [Related]
14. [Genetic variants of CYP1B1 and WDR36 in the patients with primary congenital glaucoma and primary open angle glaucoma from Saint-Petersburg]. Motushchuk AE; Komarova TIu; Grudinina NA; Rakhmanov VV; Mandel'shtam MIu; Astakhov IuS; Vasil'ev VB Genetika; 2009 Dec; 45(12):1659-67. PubMed ID: 20198978 [TBL] [Abstract][Full Text] [Related]
15. Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population. Millá E; Mañé B; Duch S; Hernan I; Borràs E; Planas E; Dias Mde S; Carballo M; Gamundi MJ; Mol Vis; 2013; 19():1707-22. PubMed ID: 23922489 [TBL] [Abstract][Full Text] [Related]
16. Genetics of primary glaucoma. Khan AO Curr Opin Ophthalmol; 2011 Sep; 22(5):347-55. PubMed ID: 21730848 [TBL] [Abstract][Full Text] [Related]
17. Molecular and clinical evaluation of primary congenital glaucoma in Kuwait. Alfadhli S; Behbehani A; Elshafey A; Abdelmoaty S; Al-Awadi S Am J Ophthalmol; 2006 Mar; 141(3):512-6. PubMed ID: 16490498 [TBL] [Abstract][Full Text] [Related]
18. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree. Ramprasad VL; Sripriya S; Ronnie G; Nancarrow D; Saxena S; Hemamalini A; Kumar D; Vijaya L; Kumaramanickavel G Mol Vis; 2005 Nov; 11():934-40. PubMed ID: 16288197 [TBL] [Abstract][Full Text] [Related]
19. CYP1B1 and MYOC mutations in 116 Chinese patients with primary congenital glaucoma. Chen Y; Jiang D; Yu L; Katz B; Zhang K; Wan B; Sun X Arch Ophthalmol; 2008 Oct; 126(10):1443-7. PubMed ID: 18852424 [TBL] [Abstract][Full Text] [Related]
20. Sturge-Weber syndrome with congenital glaucoma and cytochrome P450 (CYP1B1) gene mutations. Tanwar M; Sihota R; Dada T; Gupta V; Das TK; Yadav U; Dada R J Glaucoma; 2010 Aug; 19(6):398-404. PubMed ID: 20051892 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]