198 related articles for article (PubMed ID: 30426773)
1. Recurrent
Chen DD; Yang T; Zhu SQ
Eur J Ophthalmol; 2020 Jan; 30(1):181-188. PubMed ID: 30426773
[TBL] [Abstract][Full Text] [Related]
2. Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract.
Lin Y; Gao H; Zhu Y; Chen C; Li T; Liu B; Lyu C; Huang Y; Li H; Wu Q; Jin C; Liang X; Huang X; Lu L
Mol Med Rep; 2018 Nov; 18(5):4439-4445. PubMed ID: 30221735
[TBL] [Abstract][Full Text] [Related]
3. A novel PAX6 mutation in a large Chinese family with aniridia and congenital cataract.
Cai F; Zhu J; Chen W; Ke T; Wang F; Tu X; Zhang Y; Jin R; Wu X
Mol Vis; 2010 Jun; 16():1141-5. PubMed ID: 20664694
[TBL] [Abstract][Full Text] [Related]
4. A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family.
Jin C; Wang Q; Li J; Zhu Y; Shentu X; Yao K
Mol Vis; 2012; 18():465-70. PubMed ID: 22393272
[TBL] [Abstract][Full Text] [Related]
5. Mutation analysis of paired box 6 gene in inherited aniridia in northern China.
Chen P; Zang X; Sun D; Wang Y; Wang Y; Zhao X; Zhang M; Xie L
Mol Vis; 2013; 19():1169-77. PubMed ID: 23734086
[TBL] [Abstract][Full Text] [Related]
6. A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridia.
Liu X; Wu Y; Miao Z; Zhang H; Gong B; Zhu X; Huang L; Shi Y; Hao F; Ma S; Lin H; Wang L; Yang Z
Ophthalmic Genet; 2018 Aug; 39(4):428-436. PubMed ID: 29902091
[TBL] [Abstract][Full Text] [Related]
7. A novel PAX6 deletion in a Chinese family with congenital aniridia.
Chen JH; Lin W; Sun G; Huang C; Huang Y; Chen H; Pang CP; Zhang M
Mol Vis; 2012; 18():989-95. PubMed ID: 22550392
[TBL] [Abstract][Full Text] [Related]
8. Novel Intragenic
Boese EA; Tollefson MR; Schnieders MJ; Darbro BW; Alward WLM; Fingert JH
Curr Eye Res; 2020 Jan; 45(1):91-96. PubMed ID: 31361967
[No Abstract] [Full Text] [Related]
9. A novel PAX6 gene mutation in a Chinese family with aniridia.
Song S; Liu Y; Guo S; Zhang L; Zhang X; Wang S; Lu A; Li L
Mol Vis; 2005 May; 11():335-7. PubMed ID: 15889018
[TBL] [Abstract][Full Text] [Related]
10. Detection of a novel PAX6 variant in a Chinese family with multiple ocular abnormalities.
Ouyang J; Cai Z; Guo Y; Nie F; Cao M; Duan X
BMC Ophthalmol; 2022 Jan; 22(1):28. PubMed ID: 35034608
[TBL] [Abstract][Full Text] [Related]
11. A novel 4.25 kb heterozygous deletion in PAX6 in a Chinese Han family with congenital aniridia combined with cataract and nystagmus.
Qian T; Chen C; Li C; Gong Q; Liu K; Wang G; Schrauwen I; Xu X
BMC Ophthalmol; 2021 Oct; 21(1):353. PubMed ID: 34610801
[TBL] [Abstract][Full Text] [Related]
12. Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
Dansault A; David G; Schwartz C; Jaliffa C; Vieira V; de la Houssaye G; Bigot K; Catin F; Tattu L; Chopin C; Halimi P; Roche O; Van Regemorter N; Munier F; Schorderet D; Dufier JL; Marsac C; Ricquier D; Menasche M; Penfornis A; Abitbol M
Mol Vis; 2007 Apr; 13():511-23. PubMed ID: 17417613
[TBL] [Abstract][Full Text] [Related]
13. Extension of the mutation spectrum of PAX6 from three Chinese congenital aniridia families and identification of male gonadal mosaicism.
Bai Z; Kong X
Mol Genet Genomic Med; 2018 Nov; 6(6):1053-1067. PubMed ID: 30334364
[TBL] [Abstract][Full Text] [Related]
14. Identification of a novel PAX6 mutation in a Chinese family with aniridia.
Qiu JJ; Zhang Q; Geng ZX; Liu M; Zhong ZL; Chen JJ; Liu F
BMC Ophthalmol; 2019 Jan; 19(1):10. PubMed ID: 30621664
[TBL] [Abstract][Full Text] [Related]
15. A novel de novo duplication mutation of PAX6 in a Chinese family with aniridia and other ocular abnormalities.
Zhuang J; Chen X; Tan Z; Zhu Y; Zhao K; Yang J
Sci Rep; 2014 May; 4():4836. PubMed ID: 24787241
[TBL] [Abstract][Full Text] [Related]
16. A Novel
Xiao Y; Liu X; Yang C; Liu L; Guo X; Wang Q; Gong B
Genet Test Mol Biomarkers; 2019 Jul; 23(7):495-500. PubMed ID: 31161946
[No Abstract] [Full Text] [Related]
17. Large novel deletions detected in Chinese families with aniridia: correlation between genotype and phenotype.
Zhang X; Zhang Q; Tong Y; Dai H; Zhao X; Bai F; Xu L; Li Y
Mol Vis; 2011 Feb; 17():548-57. PubMed ID: 21364908
[TBL] [Abstract][Full Text] [Related]
18. [Mutation analysis of the PAX6 gene in a family with congenital aniridia and cataract].
Lin Y; Li J; Yang Y; Yang JY; Zhang B; Tang X; Liu XQ; Lu F; Yang ZL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):542-5. PubMed ID: 19806578
[TBL] [Abstract][Full Text] [Related]
19. A novel PAX6 mutation in Chinese patients with severe congenital aniridia.
He Y; Pan Z; Luo F
Curr Eye Res; 2012 Oct; 37(10):879-83. PubMed ID: 22621390
[TBL] [Abstract][Full Text] [Related]
20. Familial congenital cataract, coloboma, and nystagmus phenotype with variable expression caused by mutation in
Goolam S; Carstens N; Ross M; Bentley D; Lopes M; Peden J; Kingsbury Z; Tsogka E; Barlow R; Carmichael TR; Ramsay M; Williams SE
Mol Vis; 2018; 24():407-413. PubMed ID: 29930474
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
