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D A Mackey

Showing results (41-50 of 65) with videos related to

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Ophthalmic Epidemiology|December 29, 2007
The association between maternal smoking in pregnancy, other early life characteristics and childhood vision: the Twins Eye Study in TasmaniaA L Ponsonby, S A Brown, L S Kearns, et al.
Clinical Genetics|August 28, 2007
Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucomaD P Dimasi, A W Hewitt, T Straga, et al.
Eye (London, England)|May 2, 2003
Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virusD A Mackey, J H Fingert, J Z Luzhansky, et al.
The British Journal of Ophthalmology|July 11, 2006
Nail-patella syndrome and its association with glaucoma: a review of eight familiesZ Mimiwati, D A Mackey, J E Craig, et al.
Journal of Medical Genetics|August 6, 2002
Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of diseaseN J Marchbank, J E Craig, J P Leek, et al.
The Journal of Laryngology and Otology|August 5, 2021
Olfactory dysfunction at six months after coronavirus disease 2019 infectionS R Leedman, M Sheeraz, P G Sanfilippo, et al.
Journal of Medical Genetics|August 3, 2004
A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetranceK P Burdon, M G Wirth, D A Mackey, et al.
Eye (London, England)|November 27, 2010
Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutationsA C Cohn, C Turnbull, J B Ruddle, et al.
The British Journal of Ophthalmology|December 25, 2003
Investigation of crystallin genes in familial cataract, and report of two disease associated mutationsK P Burdon, M G Wirth, D A Mackey, et al.
American Journal of Human Genetics|August 1, 1996
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathyD A Mackey, R J Oostra, T Rosenberg, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
Ophthalmic Epidemiology|December 29, 2007
The association between maternal smoking in pregnancy, other early life characteristics and childhood vision: the Twins Eye Study in TasmaniaA L Ponsonby, S A Brown, L S Kearns, et al.
Clinical Genetics|August 28, 2007
Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucomaD P Dimasi, A W Hewitt, T Straga, et al.
Eye (London, England)|May 2, 2003
Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virusD A Mackey, J H Fingert, J Z Luzhansky, et al.
The British Journal of Ophthalmology|July 11, 2006
Nail-patella syndrome and its association with glaucoma: a review of eight familiesZ Mimiwati, D A Mackey, J E Craig, et al.
Journal of Medical Genetics|August 6, 2002
Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of diseaseN J Marchbank, J E Craig, J P Leek, et al.
The Journal of Laryngology and Otology|August 5, 2021
Olfactory dysfunction at six months after coronavirus disease 2019 infectionS R Leedman, M Sheeraz, P G Sanfilippo, et al.
Journal of Medical Genetics|August 3, 2004
A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetranceK P Burdon, M G Wirth, D A Mackey, et al.
Eye (London, England)|November 27, 2010
Best's macular dystrophy in Australia: phenotypic profile and identification of novel BEST1 mutationsA C Cohn, C Turnbull, J B Ruddle, et al.
The British Journal of Ophthalmology|December 25, 2003
Investigation of crystallin genes in familial cataract, and report of two disease associated mutationsK P Burdon, M G Wirth, D A Mackey, et al.
American Journal of Human Genetics|August 1, 1996
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathyD A Mackey, R J Oostra, T Rosenberg, et al.
Pageof 7