233 related articles for article (PubMed ID: 25900864)
1. Early onset ectopia lentis due to a FBN1 mutation with non-penetrance.
Zhang L; Lai YH; Capasso JE; Han S; Levin AV
Am J Med Genet A; 2015 Jun; 167(6):1365-8. PubMed ID: 25900864
[TBL] [Abstract][Full Text] [Related]
2. A recurrent FBN1 mutation in an autosomal dominant ectopia lentis family of Indian origin.
Vanita V; Singh JR; Singh D; Varon R; Robinson PN; Sperling K
Mol Vis; 2007 Oct; 13():2035-40. PubMed ID: 18079676
[TBL] [Abstract][Full Text] [Related]
3. A FBN1 mutation association with different phenotypes of Marfan syndrome in a Chinese family.
Li Y; Xu J; Chen M; Du B; Li Q; Xing Q; Zhang Y
Clin Chim Acta; 2016 Sep; 460():102-6. PubMed ID: 27353645
[TBL] [Abstract][Full Text] [Related]
4. The revised ghent nosology; reclassifying isolated ectopia lentis.
Chandra A; Patel D; Aragon-Martin JA; Pinard A; Collod-Béroud G; Comeglio P; Boileau C; Faivre L; Charteris D; Child AH; Arno G
Clin Genet; 2015 Mar; 87(3):284-7. PubMed ID: 24635535
[TBL] [Abstract][Full Text] [Related]
5. Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome.
Loeys B; Nuytinck L; Delvaux I; De Bie S; De Paepe A
Arch Intern Med; 2001 Nov; 161(20):2447-54. PubMed ID: 11700157
[TBL] [Abstract][Full Text] [Related]
6. Ectopia lentis as the presenting and primary feature in Marfan syndrome.
Zadeh N; Bernstein JA; Niemi AK; Dugan S; Kwan A; Liang D; Hyland JC; Hoyme HE; Hudgins L; Manning MA
Am J Med Genet A; 2011 Nov; 155A(11):2661-8. PubMed ID: 21932315
[TBL] [Abstract][Full Text] [Related]
7. The roles of two novel FBN1 gene mutations in the genotype-phenotype correlations of Marfan syndrome and ectopia lentis patients with marfanoid habitus.
Li D; Yu J; Gu F; Pang X; Ma X; Li R; Liu N; Ma X
Genet Test; 2008 Jun; 12(2):325-30. PubMed ID: 18471089
[TBL] [Abstract][Full Text] [Related]
8. A genotype-phenotype comparison of ADAMTSL4 and FBN1 in isolated ectopia lentis.
Chandra A; Aragon-Martin JA; Hughes K; Gati S; Reddy MA; Deshpande C; Cormack G; Child AH; Charteris DG; Arno G
Invest Ophthalmol Vis Sci; 2012 Jul; 53(8):4889-96. PubMed ID: 22736615
[TBL] [Abstract][Full Text] [Related]
9. Ophthalmic findings in a family with early-onset isolated ectopia lentis and the p.Arg62Cys mutation of the fibrillin-1 gene (FBN1).
Zhao JH; Jin TB; Liu QB; Chen C; Hu HT
Ophthalmic Genet; 2013; 34(1-2):21-6. PubMed ID: 22950452
[TBL] [Abstract][Full Text] [Related]
10. [Recurrent N1173K mutation in FBN1 gene in a Chinese family with ectopia lentis].
Feng XL; Li ND; Wang LM; Wang YC; Zhao KX
Zhonghua Yan Ke Za Zhi; 2012 Aug; 48(8):728-32. PubMed ID: 23141514
[TBL] [Abstract][Full Text] [Related]
11. Ectopia lentis phenotypes and the FBN1 gene.
Adès LC; Holman KJ; Brett MS; Edwards MJ; Bennetts B
Am J Med Genet A; 2004 Apr; 126A(3):284-9. PubMed ID: 15054843
[TBL] [Abstract][Full Text] [Related]
12. Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome.
Kainulainen K; Karttunen L; Puhakka L; Sakai L; Peltonen L
Nat Genet; 1994 Jan; 6(1):64-9. PubMed ID: 8136837
[TBL] [Abstract][Full Text] [Related]
13. Novel FBN1 mutations associated with predominant ectopia lentis and marfanoid habitus in Chinese patients.
Jin C; Yao K; Jiang J; Tang X; Shentu X; Wu R
Mol Vis; 2007 Jul; 13():1280-4. PubMed ID: 17679947
[TBL] [Abstract][Full Text] [Related]
14. Identification of a novel FBN1 mutation in a Chinese family with isolated ectopia lentis.
Liang C; Fan W; Wu S; Liu Y
Mol Vis; 2011; 17():3481-5. PubMed ID: 22219643
[TBL] [Abstract][Full Text] [Related]
15. Novel mutation in FBN1 causes ectopia lentis and varicose great saphenous vein in one Chinese autosomal dominant family.
Fu Q; Liu P; Lu Q; Wang F; Wang H; Shen W; Xu F; Liu L; Sergeev YV; Sui R
Mol Vis; 2014; 20():812-21. PubMed ID: 24940037
[TBL] [Abstract][Full Text] [Related]
16. Novel p.G1344E mutation in
Yang Y; Zhou YL; Yao TT; Pan H; Gu P; Wang ZY
Br J Ophthalmol; 2021 Mar; 105(3):341-347. PubMed ID: 32404357
[TBL] [Abstract][Full Text] [Related]
17. Role of ADAMTSL4 mutations in FBN1 mutation-negative ectopia lentis patients.
Aragon-Martin JA; Ahnood D; Charteris DG; Saggar A; Nischal KK; Comeglio P; Chandra A; Child AH; Arno G
Hum Mutat; 2010 Aug; 31(8):E1622-31. PubMed ID: 20564469
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel FBN1 gene mutation in a large Pakistani family with Marfan syndrome.
Micheal S; Khan MI; Akhtar F; Weiss MM; Islam F; Ali M; Qamar R; Maugeri A; den Hollander AI
Mol Vis; 2012; 18():1918-26. PubMed ID: 22876116
[TBL] [Abstract][Full Text] [Related]
19. Clinical and linkage study of a large family with simple ectopia lentis linked to FBN1.
Edwards MJ; Challinor CJ; Colley PW; Roberts J; Partington MW; Hollway GE; Kozman HM; Mulley JC
Am J Med Genet; 1994 Oct; 53(1):65-71. PubMed ID: 7802039
[TBL] [Abstract][Full Text] [Related]
20. [Novel mutation of fibrillin 1 gene cause ectopia lentis in a Chinese family].
Sui RF; Wei HB; Zhao JL; Hu SY; Wang B; Huang SZ; Dong M
Zhonghua Yan Ke Za Zhi; 2004 Dec; 40(12):828-31. PubMed ID: 15733436
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]