Lloyd IC - Search Results

1

Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach.

Musleh M, Hall G, Lloyd IC, Gillespie RL, Waller S, Douzgou S, Clayton-Smith J, Kehdi E, Black GC, Ashworth J. Musleh M, et al. Among authors: lloyd ic. Eye (Lond). 2016 Sep;30(9):1175-81. doi: 10.1038/eye.2016.105. Epub 2016 Jun 17. Eye (Lond). 2016. PMID: 27315345 Free PMC article.

2

Neonatal cataract: aetiology, pathogenesis and management.

Lloyd IC, Goss-Sampson M, Jeffrey BG, Kriss A, Russell-Eggitt I, Taylor D. Lloyd IC, et al. Eye (Lond). 1992;6 ( Pt 2):184-96. doi: 10.1038/eye.1992.37. Eye (Lond). 1992. PMID: 1624043 Review.

3

Anterior segment dysgenesis in mosaic Turner syndrome.

Lloyd IC, Haigh PM, Clayton-Smith J, Clayton P, Price DA, Ridgway AE, Donnai D. Lloyd IC, et al. Br J Ophthalmol. 1997 Aug;81(8):639-43. doi: 10.1136/bjo.81.8.639. Br J Ophthalmol. 1997. PMID: 9349149 Free PMC article.

4

A mutation in the RIEG1 gene associated with Peters' anomaly.

Doward W, Perveen R, Lloyd IC, Ridgway AE, Wilson L, Black GC. Doward W, et al. Among authors: lloyd ic. J Med Genet. 1999 Feb;36(2):152-5. J Med Genet. 1999. PMID: 10051017 Free PMC article.

5

Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis.

Black GC, Perveen R, Bonshek R, Cahill M, Clayton-Smith J, Lloyd IC, McLeod D. Black GC, et al. Among authors: lloyd ic. Hum Mol Genet. 1999 Oct;8(11):2031-5. doi: 10.1093/hmg/8.11.2031. Hum Mol Genet. 1999. PMID: 10484772

6

Apple peel atresia in association with bilateral colobomatous malformation of the optic nerve heads, dysmorphic features, and learning disability - a new syndrome?

Waters FM, Lloyd IC, Clayton-Smith J. Waters FM, et al. Among authors: lloyd ic. Ophthalmic Genet. 2000 Jun;21(2):117-21. Ophthalmic Genet. 2000. PMID: 10916186

7

Phenotypic variability and asymmetry of Rieger syndrome associated with PITX2 mutations.

Perveen R, Lloyd IC, Clayton-Smith J, Churchill A, van Heyningen V, Hanson I, Taylor D, McKeown C, Super M, Kerr B, Winter R, Black GC. Perveen R, et al. Among authors: lloyd ic. Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2456-60. Invest Ophthalmol Vis Sci. 2000. PMID: 10937553

8

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: lloyd ic. 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.

9

Autosomal dominant brachydactyly, coloboma and anterior segment dysgenesis.

Quinn SM, Black GC, Biswas S, Clayton-Smith J, Lloyd IC. Quinn SM, et al. Among authors: lloyd ic. Ophthalmic Genet. 2004 Dec;25(4):277-83. doi: 10.1080/13816810490902684. Ophthalmic Genet. 2004. PMID: 15621880

10

The ocular features of the mucopolysaccharidoses.

Ashworth JL, Biswas S, Wraith E, Lloyd IC. Ashworth JL, et al. Among authors: lloyd ic. Eye (Lond). 2006 May;20(5):553-63. doi: 10.1038/sj.eye.6701921. Eye (Lond). 2006. PMID: 15905869

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