A constitutional mutation within the retinoblastoma gene detected by PFGE
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1994.tb03981.x/fullpdf
Reference26 articles.
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2. Physical map around the retinoblastoma gene: possible genomic imprinting suggested by Nrul digestion;Blanquet;Genomics,1991
3. The clinical, genetic and dystrophin characteristics of Becker Muscular Dystrophy: correlation of phenotype with genetic and protein abnormalities;Bushby;J Neurol,1993
4. Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene;Canning;Proc Natl Acad Sci USA,1989
5. Deletion of the esterase D locus from a survey of 200 retinoblastoma patients;Cowell;Hum Genet,1986
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1. A novel translocation t(11;13) (q21;q14.2) in a child with suprasellar primitive neuroectodermal tumor and retinoblastoma;Ophthalmic Genetics;2012-08-27
2. Sensitive and Efficient Detection of RB1 Gene Mutations Enhances Care for Families with Retinoblastoma;The American Journal of Human Genetics;2003-02
3. Characterization by FISH of a t(5;13) in a patient with bilateral retinoblastoma;Cancer Genetics and Cytogenetics;1997-07
4. Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.;Journal of Medical Genetics;1994-12-01
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