Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype
- Author
- ONADIM, Z; HOGG, A; BAIRD, P. N; COWELL, J. K
Inst. child health, imperial cancer res. fund oncology group, London WC1N 1EH, United Kingdom - Source
Proceedings of the National Academy of Sciences of the United States of America. 1992, Vol 89, Num 13, pp 6177-6181 ; ref : 37 ref
- CODEN
- PNASA6
- ISSN
- 0027-8424
- Scientific domain
- Multidisciplinary
- Publisher
- National Academy of Sciences of the United States of America, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Carcinogenèse Etude familiale Mutation Pathogénie Phénotype Rétinoblastome Gène RB1 Gène suppresseur tumeur Polymorphisme conformation simple brin
- Keyword (en)
- Carcinogenesis Family study Mutation Pathogenesis Phenotype Retinoblastoma Tumor suppressor gene
- Keyword (es)
- Carcinogénesis Estudio familiar Mutación Patogenia Fenotipo Retinoblastoma
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B04 Tumors / 002B04E Carcinogenesis, carcinogens and anticarcinogens / 002B04E05 Foods and miscellaneous
- Discipline
- Tumours
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 5441370
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1073/pnas.89.13.6177 
https://dx.doi.org/10.1073/pnas.89.13.6177
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