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4. [An attempt to locate the gene for congenital cataracts using linkage analysis]. Ginter EK; Petrin AN; Spitsyn VA; Rogaev EI Genetika; 1991 Oct; 27(10):1840-9. PubMed ID: 1778455 [TBL] [Abstract][Full Text] [Related]
5. Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations. Forshew T; Johnson CA; Khaliq S; Pasha S; Willis C; Abbasi R; Tee L; Smith U; Trembath RC; Mehdi SQ; Moore AT; Maher ER Hum Genet; 2005 Sep; 117(5):452-9. PubMed ID: 15959809 [TBL] [Abstract][Full Text] [Related]
6. Classification of hereditary cataracts in children by linkage analysis. Maumenee IH Ophthalmology; 1979 Sep; 86(9):1554-8. PubMed ID: 121767 [TBL] [Abstract][Full Text] [Related]
8. A new locus for autosomal dominant congenital cataracts maps to chromosome 3. Kramer PL; LaMorticella D; Schilling K; Billingslea AM; Weleber RG; Litt M Invest Ophthalmol Vis Sci; 2000 Jan; 41(1):36-9. PubMed ID: 10634598 [TBL] [Abstract][Full Text] [Related]
9. Mapping of the human CP49 gene and identification of an intragenic polymorphic marker to allow genetic linkage analysis in autosomal dominant congenital cataract. Carter JM; McLean WH; West S; Quinlan RA Biochem Biophys Res Commun; 2000 Apr; 270(2):432-6. PubMed ID: 10753642 [TBL] [Abstract][Full Text] [Related]
11. A deletion mutation in the betaA1/A3 crystallin gene ( CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family. Qi Y; Jia H; Huang S; Lin H; Gu J; Su H; Zhang T; Gao Y; Qu L; Li D; Li Y Hum Genet; 2004 Jan; 114(2):192-7. PubMed ID: 14598164 [TBL] [Abstract][Full Text] [Related]
12. Congenital cataracts: gene mapping. He W; Li S Hum Genet; 2000 Jan; 106(1):1-13. PubMed ID: 10982175 [TBL] [Abstract][Full Text] [Related]
13. Further genetic heterogeneity for autosomal dominant human sutural cataracts. Klopp N; Héon E; Billingsley G; Illig T; Wjst M; Rudolph G; Graw J Ophthalmic Res; 2003; 35(2):71-7. PubMed ID: 12646746 [TBL] [Abstract][Full Text] [Related]
15. A missense mutation S228P in the CRYBB1 gene causes autosomal dominant congenital cataract. Wang J; Ma X; Gu F; Liu NP; Hao XL; Wang KJ; Wang NL; Zhu SQ Chin Med J (Engl); 2007 May; 120(9):820-4. PubMed ID: 17531125 [TBL] [Abstract][Full Text] [Related]
16. The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes. McKay JD; Patterson B; Craig JE; Russell-Eggitt IM; Wirth MG; Burdon KP; Hewitt AW; Cohn AC; Kerdraon Y; Mackey DA Br J Ophthalmol; 2005 Jul; 89(7):831-4. PubMed ID: 15965161 [TBL] [Abstract][Full Text] [Related]
17. Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1. Magenis RE; Donlon T; Parks M; Rivas ML; Lovrien EW Cytogenet Cell Genet; 1978; 22(1-6):327-9. PubMed ID: 752496 [No Abstract] [Full Text] [Related]
18. A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2. Abouzeid H; Meire FM; Osman I; ElShakankiri N; Bolay S; Munier FL; Schorderet DF Ophthalmology; 2009 Jan; 116(1):154-162.e1. PubMed ID: 19004499 [TBL] [Abstract][Full Text] [Related]
19. A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts. Ma X; Li FF; Wang SZ; Gao C; Zhang M; Zhu SQ Mol Vis; 2008; 14():1906-11. PubMed ID: 18958306 [TBL] [Abstract][Full Text] [Related]
20. [Gene mapping and mutation detection in a family with congenital nuclear cataract]. Liu P; Zhang L; Ouyang S; Gao LH; He L; Fu SB Zhonghua Yan Ke Za Zhi; 2009 Mar; 45(3):234-8. PubMed ID: 19575918 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]