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Correction: Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.
Lenassi E, Clayton-Smith J, Douzgou S, Ramsden SC, Ingram S, Hall G, Hardcastle CL, Fletcher TA, Taylor RL, Ellingford JM, Newman WD, Fenerty C, Sharma V, Lloyd IC, Biswas S, Ashworth JL, Black GC, Sergouniotis PI. Lenassi E, et al. Among authors: biswas s. Genet Med. 2021 Oct;23(10):2023. doi: 10.1038/s41436-020-01068-8. Genet Med. 2021. PMID: 33353976 Free PMC article. No abstract available.
Oculocutaneous albinism.
Biswas S, Lloyd IC. Biswas S, et al. Arch Dis Child. 1999 Jun;80(6):565-9. doi: 10.1136/adc.80.6.565. Arch Dis Child. 1999. PMID: 10332009 Free PMC article. Review. No abstract available.
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.
Biswas S, Munier FL, Yardley J, Hart-Holden N, Perveen R, Cousin P, Sutphin JE, Noble B, Batterbury M, Kielty C, Hackett A, Bonshek R, Ridgway A, McLeod D, Sheffield VC, Stone EM, Schorderet DF, Black GC. Biswas S, et al. Hum Mol Genet. 2001 Oct 1;10(21):2415-23. doi: 10.1093/hmg/10.21.2415. Hum Mol Genet. 2001. PMID: 11689488
The ophthalmic findings in Cohen syndrome.
Chandler KE, Biswas S, Lloyd IC, Parry N, Clayton-Smith J, Black GC. Chandler KE, et al. Among authors: biswas s. Br J Ophthalmol. 2002 Dec;86(12):1395-8. doi: 10.1136/bjo.86.12.1395. Br J Ophthalmol. 2002. PMID: 12446373 Free PMC article.
The ocular features of the mucopolysaccharidoses.
Ashworth JL, Biswas S, Wraith E, Lloyd IC. Ashworth JL, et al. Among authors: biswas s. Eye (Lond). 2006 May;20(5):553-63. doi: 10.1038/sj.eye.6701921. Eye (Lond). 2006. PMID: 15905869
Mucopolysaccharidoses and the eye.
Ashworth JL, Biswas S, Wraith E, Lloyd IC. Ashworth JL, et al. Among authors: biswas s. Surv Ophthalmol. 2006 Jan-Feb;51(1):1-17. doi: 10.1016/j.survophthal.2005.11.007. Surv Ophthalmol. 2006. PMID: 16414358 Review.
4,045 results