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Items where Author is "Dimasi, DP"

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Number of items: 5.

Article

Balaratnasingam, C, Morgan, WH, Nelson, J, Mackey, DA, Dimasi, DP and Lam, G 2007 , 'Abnormal iris processes may be a marker of glaucoma gene carrier status in some cases of primary infantile glaucoma' , Ophthalmic Genetics, vol. 28, no. 3 , pp. 157-162 , doi: https://doi.org/10.1080/13816810701503715.

Burdon, KP, Sharma, S, Chen, CS, Dimasi, DP, Mackey, DA and Craig, JE 2007 , 'A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site' , Nature, vol. 28, no. 7 , p. 742 .

Dimasi, DP, Hewitt, AW, Straga, T, Pater, J, MacKinnon, JR, Elder, JE, Casey, T, Mackey, DA and Craig, JE 2007 , 'Prevalence of CYP1B1 mutations in Australian patients with primary congenial glaucoma' , Clinical Genetics, vol. 72, no. 3 , pp. 255-260 , doi: https://doi.org/10.1111/j.1399-0004.2007.00864.x.

Hewitt, AW, Heon, E, Craig, JE, Mackey, DA, Bennett, SL, Richards, JE, Dimasi, DP, Booth, AP, Inglehearn, CF, Anwar, R, Yamamoto, T and Fingert, JH 2007 , 'Myocilin Gly252Arg mutation and glaucoma of intermediate severity in caucasioan individuals' , Archives of Ophthalmology, vol. 125, no. 1 , pp. 98-104 .

Hewitt, AW, Sharma, Shiwani, Burdon, KP, Wang, JJ, Baird, PN, Dimasi, DP, Mackey, DA, Mitchell, P and Craig, JE 2007 , 'Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people' , Human Molecular Genetics, vol. 17, no. 5 , pp. 710-716 , doi: https://doi.org/10.1093/hmg/ddm342.

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