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Host resistance to the gene for retinoblastoma Ei MATSUNAGA 1 1Department of Human Genetics, National Institute of Genetics pp.1096-1104
Published Date 1979/12/10
DOI https://doi.org/10.11477/mf.1431905118
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Abstract

Retinoblastoma is a malignant neoplasm of the eye affecting one per ca. 20,000 infants. There are two forms, hereditary and nonhereditary. The nonhereditary form, which comprises a majority of sporadic unilateral cases, represents about 60% of all retinoblastomas. The remaining 40% are hereditary and due to an autosomal dominant gene with incomplete penetrance and expressivity. While all bilateral cases, whether sporadic or familial, are to be regarded as hereditary, a gene carrier can be unilaterally affected or remain unaffected.


Copyright © 1979, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1243 印刷版ISSN 0001-8724 医学書院

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