Full text
PDF
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bodmer W. F., Bailey C. J., Bodmer J., Bussey H. J., Ellis A., Gorman P., Lucibello F. C., Murday V. A., Rider S. H., Scambler P. Localization of the gene for familial adenomatous polyposis on chromosome 5. Nature. 1987 Aug 13;328(6131):614–616. doi: 10.1038/328614a0. [DOI] [PubMed] [Google Scholar]
- Chapman P. D., Church W., Burn J., Gunn A. Congenital hypertrophy of retinal pigment epithelium: a sign of familial adenomatous polyposis. BMJ. 1989 Feb 11;298(6670):353–354. doi: 10.1136/bmj.298.6670.353. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Emery A. E., Brough C., Crawfurd M., Harper P., Harris R., Oakshott G. A report on genetic registers. Based on the report of the Clinical Genetics Society Working Party. J Med Genet. 1978 Dec;15(6):435–442. doi: 10.1136/jmg.15.6.435. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Friend S. H., Bernards R., Rogelj S., Weinberg R. A., Rapaport J. M., Albert D. M., Dryja T. P. A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma. Nature. 1986 Oct 16;323(6089):643–646. doi: 10.1038/323643a0. [DOI] [PubMed] [Google Scholar]
- Greger V., Kerst S., Messmer E., Höpping W., Passarge E., Horsthemke B. Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma. J Med Genet. 1988 Apr;25(4):217–221. doi: 10.1136/jmg.25.4.217. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Huson S. M., Harper P. S., Hourihan M. D., Cole G., Weeks R. D., Compston D. A. Cerebellar haemangioblastoma and von Hippel-Lindau disease. Brain. 1986 Dec;109(Pt 6):1297–1310. doi: 10.1093/brain/109.6.1297. [DOI] [PubMed] [Google Scholar]
- Scheffer H., Kema I. P., Kondo I., van der Veen A. Y., Ikeuchi T., Buys C. H. Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease. Hum Genet. 1987 Dec;77(4):335–337. doi: 10.1007/BF00291421. [DOI] [PubMed] [Google Scholar]
- Seizinger B. R., Rouleau G. A., Ozelius L. J., Lane A. H., Farmer G. E., Lamiell J. M., Haines J., Yuen J. W., Collins D., Majoor-Krakauer D. Von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma. Nature. 1988 Mar 17;332(6161):268–269. doi: 10.1038/332268a0. [DOI] [PubMed] [Google Scholar]
- Simpson N. E., Kidd K. K., Goodfellow P. J., McDermid H., Myers S., Kidd J. R., Jackson C. E., Duncan A. M., Farrer L. A., Brasch K. Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage. Nature. 1987 Aug 6;328(6130):528–530. doi: 10.1038/328528a0. [DOI] [PubMed] [Google Scholar]