Moore AT - Search Results

1

Evaluation of molecular genetic diagnosis in the management of familial adenomatous polyposis coli: a population based study.

Maher ER, Barton DE, Slatter R, Koch DJ, Jones MH, Nagase H, Payne SJ, Charles SJ, Moore AT, Nakamura Y, et al. Maher ER, et al. Among authors: moore at. J Med Genet. 1993 Aug;30(8):675-8. doi: 10.1136/jmg.30.8.675. J Med Genet. 1993. PMID: 8105087 Free PMC article.

2

Incidence and significance of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial adenomatous polyposis coli (FAPC).

Moore AT, Maher ER, Koch DJ, Charles SJ. Moore AT, et al. Ophthalmic Paediatr Genet. 1992 Jun;13(2):67-71. doi: 10.3109/13816819209087606. Ophthalmic Paediatr Genet. 1992. PMID: 1323091

3

Genetic mapping of X linked ocular albinism: linkage analysis in British families.

Charles SJ, Moore AT, Yates JR. Charles SJ, et al. Among authors: moore at. J Med Genet. 1992 Aug;29(8):552-4. doi: 10.1136/jmg.29.8.552. J Med Genet. 1992. PMID: 1355560 Free PMC article.

4

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

Zhang Y, McMahon R, Charles SJ, Green JS, Moore AT, Barton DE, Yates JR. Zhang Y, et al. Among authors: moore at. J Med Genet. 1993 Nov;30(11):923-5. doi: 10.1136/jmg.30.11.923. J Med Genet. 1993. PMID: 8301646 Free PMC article.

5

Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.

Maher ER, Webster AR, Richards FM, Green JS, Crossey PA, Payne SJ, Moore AT. Maher ER, et al. Among authors: moore at. J Med Genet. 1996 Apr;33(4):328-32. doi: 10.1136/jmg.33.4.328. J Med Genet. 1996. PMID: 8730290 Free PMC article.

6

Improved genetic mapping of X linked retinoschisis.

George ND, Payne SJ, Bill RM, Barton DE, Moore AT, Yates JR. George ND, et al. Among authors: moore at. J Med Genet. 1996 Nov;33(11):919-22. doi: 10.1136/jmg.33.11.919. J Med Genet. 1996. PMID: 8950671 Free PMC article.

7

Results of early surgery for infantile esotropia in normal and neurologically impaired infants.

Charles SJ, Moore AT. Charles SJ, et al. Among authors: moore at. Eye (Lond). 1992;6 ( Pt 6):603-6. doi: 10.1038/eye.1992.130. Eye (Lond). 1992. PMID: 1289137

8

Genetic counselling in X-linked ocular albinism: clinical features of the carrier state.

Charles SJ, Moore AT, Grant JW, Yates JR. Charles SJ, et al. Among authors: moore at. Eye (Lond). 1992;6 ( Pt 1):75-9. doi: 10.1038/eye.1992.15. Eye (Lond). 1992. PMID: 1426406

9

Von Hippel-Lindau disease.

Maher ER, Moore AT. Maher ER, et al. Among authors: moore at. Br J Ophthalmol. 1992 Dec;76(12):743-5. doi: 10.1136/bjo.76.12.743. Br J Ophthalmol. 1992. PMID: 1486078 Free PMC article. Review. No abstract available.

10

Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction.

Charles SJ, Moore AT, Yates JR, Green T, Clark P. Charles SJ, et al. Among authors: moore at. J Med Genet. 1990 Sep;27(9):590-2. doi: 10.1136/jmg.27.9.590. J Med Genet. 1990. PMID: 2231654 Free PMC article.

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