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J E Craig

Showing results (41-50 of 53) with videos related to

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Hemoglobin|November 1, 1996
beta haplotypes of three Mexican Mestizo families with Spanish (delta beta)o-thalassemiaA R Villalobos-Arámbula, R Bustos, F J Perea, 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.
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.
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.
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.
Investigative Ophthalmology & Visual Science|January 3, 2001
Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertensionJ H Fingert, A F Clark, J E Craig, et al.
The British Journal of Ophthalmology|June 21, 2005
The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genesJ D McKay, B Patterson, J E Craig, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 19, 2000
Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in TasmaniaA I McNaught, J G Allen, D L Healey, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Hemoglobin|November 1, 1996
beta haplotypes of three Mexican Mestizo families with Spanish (delta beta)o-thalassemiaA R Villalobos-Arámbula, R Bustos, F J Perea, 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.
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.
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.
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.
Investigative Ophthalmology & Visual Science|January 3, 2001
Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertensionJ H Fingert, A F Clark, J E Craig, et al.
The British Journal of Ophthalmology|June 21, 2005
The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genesJ D McKay, B Patterson, J E Craig, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 19, 2000
Accuracy and implications of a reported family history of glaucoma: experience from the Glaucoma Inheritance Study in TasmaniaA I McNaught, J G Allen, D L Healey, et al.
American Journal of Human Genetics|February 15, 2001
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eyeD Y Nishimura, C C Searby, W L Alward, et al.
Pageof 6