Mackey DA - Search Results

1

Genetic isolates in ophthalmic diseases.

Sherwin JC, Hewitt AW, Ruddle JB, Mackey DA. Sherwin JC, et al. Among authors: mackey da. Ophthalmic Genet. 2008 Dec;29(4):149-61. doi: 10.1080/13816810802334341. Ophthalmic Genet. 2008. PMID: 19005985 Review.

2

The 'GIST' score: ranking glaucoma for genetic studies. Glaucoma Inheritance Study of Tasmania.

Coote MA, McCartney PJ, Wilkinson RM, Mackey DA. Coote MA, et al. Among authors: mackey da. Ophthalmic Genet. 1996 Dec;17(4):199-208. doi: 10.3109/13816819609057894. Ophthalmic Genet. 1996. PMID: 9010871

3

The problem of overlapping glaucoma families in the Glaucoma Inheritance Study in Tasmania (GIST).

Sack J, Healey DL, de Graaf AP, Wilkinson RM, Wilkinson CH, Barbour JM, Coote MA, McCartney PJ, Rait JL, Cooper RL, Ring MA, Mackey DA. Sack J, et al. Among authors: mackey da. Ophthalmic Genet. 1996 Dec;17(4):209-14. doi: 10.3109/13816819609057895. Ophthalmic Genet. 1996. PMID: 9010872

4

Laboratory methods in ophthalmic genetics: obtaining DNA from patients.

Dickinson JL, Sale MM, Craig JE, Mackey DA. Dickinson JL, et al. Among authors: mackey da. Ophthalmic Genet. 2001 Mar;22(1):49-60. doi: 10.1076/opge.22.1.49.2240. Ophthalmic Genet. 2001. PMID: 11262650 Review.

5

Clinical progression of keratoconus following a Vth nerve palsy.

Ruddle JB, Mackey DA, Downie NA. Ruddle JB, et al. Among authors: mackey da. Clin Exp Ophthalmol. 2003 Aug;31(4):363-5. doi: 10.1046/j.1442-9071.2003.00673.x. Clin Exp Ophthalmol. 2003. PMID: 12880466 No abstract available.

6

Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter.

Cohn AC, Kearns LS, Savarirayan R, Ryan J, Craig JE, Mackey DA. Cohn AC, et al. Among authors: mackey da. Ophthalmic Genet. 2005 Mar;26(1):45-53. doi: 10.1080/13816810590918398. Ophthalmic Genet. 2005. PMID: 15823925 Review.

7

Evidence for a novel glaucoma locus at chromosome 3p21-22.

Baird PN, Foote SJ, Mackey DA, Craig J, Speed TP, Bureau A. Baird PN, et al. Among authors: mackey da. Hum Genet. 2005 Jul;117(2-3):249-57. doi: 10.1007/s00439-005-1296-x. Epub 2005 May 20. Hum Genet. 2005. PMID: 15906098

8

Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia.

Hewitt AW, FitzGerald LM, Scotter LW, Mulhall LE, McKay JD, Mackey DA. Hewitt AW, et al. Among authors: mackey da. Clin Exp Ophthalmol. 2005 Jun;33(3):233-9. doi: 10.1111/j.1442-9071.2005.01018.x. Clin Exp Ophthalmol. 2005. PMID: 15932525

9

The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.

McKay JD, Patterson B, Craig JE, Russell-Eggitt IM, Wirth MG, Burdon KP, Hewitt AW, Cohn AC, Kerdraon Y, Mackey DA. McKay JD, et al. Among authors: mackey da. Br J Ophthalmol. 2005 Jul;89(7):831-4. doi: 10.1136/bjo.2004.058495. Br J Ophthalmol. 2005. PMID: 15965161 Free PMC article.

10

Lack of association of p53 polymorphisms and haplotypes in high and normal tension open angle glaucoma.

Dimasi DP, Hewitt AW, Green CM, Mackey DA, Craig JE. Dimasi DP, et al. Among authors: mackey da. J Med Genet. 2005 Sep;42(9):e55. doi: 10.1136/jmg.2005.032458. J Med Genet. 2005. PMID: 16140998 Free PMC article.

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