Taylor D - Search Results

1

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: taylor d. Invest Ophthalmol Vis Sci. 2000 Aug;41(9):2456-60. Invest Ophthalmol Vis Sci. 2000. PMID: 10937553

2

Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly.

Hanson IM, Fletcher JM, Jordan T, Brown A, Taylor D, Adams RJ, Punnett HH, van Heyningen V. Hanson IM, et al. Among authors: taylor d. Nat Genet. 1994 Feb;6(2):168-73. doi: 10.1038/ng0294-168. Nat Genet. 1994. PMID: 8162071

3

Frontofacionasal dysplasia: a new case and review of the phenotype.

Reardon W, Winter RM, Taylor D, Baraitser M. Reardon W, et al. Among authors: taylor d. Clin Dysmorphol. 1994 Jan;3(1):70-9. Clin Dysmorphol. 1994. PMID: 8205327 Review.

4

MRI and CT in pediatric ophthalmology: a guide to their use.

Lloyd IC, Demaerel P, Kendall BE, Taylor D. Lloyd IC, et al. Among authors: taylor d. Semin Ophthalmol. 1991 Dec;6(4):169-81. doi: 10.3109/08820539109060197. Semin Ophthalmol. 1991. PMID: 10149521 Review. No abstract available.

5

Modulation of amblyopia therapy following early surgery for unilateral congenital cataracts.

Lloyd IC, Dowler JG, Kriss A, Speedwell L, Thompson DA, Russell-Eggitt I, Taylor D. Lloyd IC, et al. Among authors: taylor d. Br J Ophthalmol. 1995 Sep;79(9):802-6. doi: 10.1136/bjo.79.9.802. Br J Ophthalmol. 1995. PMID: 7488596 Free PMC article.

6

An unknown combination of infantile spasms, retinal lesions, facial dysmorphism and limb abnormalities.

Plomp AS, Reardon W, Benton S, Taylor D, Larcher VF, Sundrum R, Winter RM. Plomp AS, et al. Among authors: taylor d. Clin Dysmorphol. 2000 Jul;9(3):189-92. doi: 10.1097/00019605-200009030-00007. Clin Dysmorphol. 2000. PMID: 10955479

7

Incidence and patterns of detection and management of childhood-onset hereditary retinal disorders in the UK.

Hamblion EL, Moore AT, Rahi JS; British Childhood Onset Hereditary Retinal Disorders Network. Hamblion EL, et al. Br J Ophthalmol. 2012 Mar;96(3):360-5. doi: 10.1136/bjo.2010.201178. Epub 2011 Jun 7. Br J Ophthalmol. 2012. PMID: 21653210

8

Aspects of albinism.

Kriss A, Russell-Eggitt I, Harris CM, Lloyd IC, Taylor D. Kriss A, et al. Among authors: taylor d. Ophthalmic Paediatr Genet. 1992 Jun;13(2):89-100. doi: 10.3109/13816819209087609. Ophthalmic Paediatr Genet. 1992. PMID: 1495771 Review.

9

Oculofacialbulbar palsy in mother and son: review of 26 reports of familial transmission within the 'Möbius spectrum of defects'.

MacDermot KD, Winter RM, Taylor D, Baraitser M. MacDermot KD, et al. Among authors: taylor d. J Med Genet. 1991 Jan;28(1):18-26. doi: 10.1136/jmg.28.1.18. J Med Genet. 1991. PMID: 1999828 Free PMC article. Review.

10

Frontonasal dysplasia with optic disc anomalies and other midline craniofacial defects: a report of six cases.

Lees MM, Hodgkins P, Reardon W, Taylor D, Stanhope R, Jones B, Hayward R, Hockley AD, Baraitser M, Winter RM. Lees MM, et al. Among authors: taylor d. Clin Dysmorphol. 1998 Jul;7(3):157-62. doi: 10.1097/00019605-199807000-00001. Clin Dysmorphol. 1998. PMID: 9689987 Review.

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