Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype.-Reference-Cited by-同舟云学术

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Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype.

Published:1992-07-01 Issue:13 Volume:89 Page:6177-6181
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Onadim Z.,Hogg A.,Baird P. N.,Cowell J. K.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Cited by 109 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. An overview of RB1 transcript alterations detected during retinoblastoma genetic screening;Ophthalmic Genetics;2023-11-06

2. Whole genome bisulfite sequencing of tumor DNA and matching cfDNA in relapsed pediatric cancer;2023-04-03

3. Novel insights into RB1 mutation;Cancer Letters;2022-10

4. The RB1 Mutation Spectrum and Genetic Management Consultation in Pediatric Patients with Retinoblastoma in Beijing, China;Risk Management and Healthcare Policy;2021-08

5. Introduction of a Variant Classification System for Analysis of Genotype-Phenotype Relationships in Heritable Retinoblastoma;Cancers;2021-03-31

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