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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. Mutation analysis of congenital cataracts in Indian families: identification of SNPS and a new causative allele in CRYBB2 gene. Santhiya ST; Manisastry SM; Rawlley D; Malathi R; Anishetty S; Gopinath PM; Vijayalakshmi P; Namperumalsamy P; Adamski J; Graw J Invest Ophthalmol Vis Sci; 2004 Oct; 45(10):3599-607. PubMed ID: 15452067 [TBL] [Abstract][Full Text] [Related]
10. Aspiration of congenital or soft cataracts: further experience. Scheie HG; Rubenstein RA; Kent RB Trans Am Ophthalmol Soc; 1966; 64():319-31. PubMed ID: 5337645 [No Abstract] [Full Text] [Related]
12. Genetic appraisal of congenital cataract. Angra SK; Rao P; Panda A; Grewal MS Indian J Ophthalmol; 1987; 35(5-6):226-32. PubMed ID: 3508777 [TBL] [Abstract][Full Text] [Related]
13. [The significance of genetic examination in the families of children with congenital cataracts]. Losan F; Nýdlová Z; Vydrová J; Maresová H Cas Lek Cesk; 1984 Nov; 123(46):1414-6. PubMed ID: 6509494 [No Abstract] [Full Text] [Related]
14. Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea. Devi RR; Vijayalakshmi P Mol Vis; 2006 Mar; 12():190-5. PubMed ID: 16604058 [TBL] [Abstract][Full Text] [Related]
15. [Surgical treatment and postoperative correction using gel contact lenses in monocular congenital cataracts]. Vymazal M; Vymazalová Z; Frysáková M Cesk Oftalmol; 1984 Sep; 40(5):293-8. PubMed ID: 6498989 [No Abstract] [Full Text] [Related]
17. [Syndrome of congenital cataracts and the bird-face anomaly. Report of 18 cases (author's transl)]. Zhang FH Zhonghua Yan Ke Za Zhi; 1981 May; 17(3):174-7. PubMed ID: 6802600 [No Abstract] [Full Text] [Related]
18. 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]
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]