11p13 deletion, Wilms' tumour, and aniridia: unusual genetic, non-ocular and ocular features of three cases.

Author:

Jotterand V,Boisjoly H M,Harnois C,Bigonesse P,Laframboise R,Gagne R,St-Pierre A

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference16 articles.

1. Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteria;Hittner, H.M.; Riccardi, V.M.; Ferrell, R.E.; Borda, R.R.; Justice, J.;AmJ Ophthalmol,1980

2. Aniridia, mental retardation and genital abnormality in two patients with 46xy I lp-;Smith, A.M.C.; Sujansky, E.; Riccardi, V.M.;Birth Defects,1977

3. Nelson LB, Spaeth GL, Nowinski TS, Margo CE, Jackson L. Aniridia. A review Surv Ophthalmol 1984; 28: 621-42.

4. Regional mapping of catalase and Wilms' tumor-aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment llpl305p1306;Narahara, K.; Kikkawa, K.; Kimira, S.;Hum Genet,1984

5. Aniridia: enzyme studies in an I lp chromosomal deletion;Bateman, J.B.; Sparkes, M.C.; Sparkes, R.S.;Invest Ophthalmol VisSci,1984

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3. Intraocular metastatic Wilms' tumour in a child;Canadian Journal of Ophthalmology;2010-12

4. Complications and Visual Prognosis in Children with Aniridia;Journal of Pediatric Ophthalmology & Strabismus;2010-07

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