Skip to main content

letter

. 1995 Feb;71(2):427. doi: 10.1038/bjc.1995.87

Molecular genetic basis of Wilms' tumour?

PMCID: PMC2033596 PMID: 7710515

427

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Baird P. N., Pritchard J., Cowell J. K. Molecular genetic analysis of chromosome 11p in familial Wilms tumour. Br J Cancer. 1994 Jun;69(6):1072–1077. doi: 10.1038/bjc.1994.210. [DOI] [PMC free article] [PubMed] [Google Scholar]
Hughes-Benzie R. M., Hunter A. G., Allanson J. E., Mackenzie A. E. Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21. 1992 Apr 15-May 1Am J Med Genet. 43(1-2):428–435. doi: 10.1002/ajmg.1320430165. [DOI] [PubMed] [Google Scholar]
Hughes-Benzie R., Allanson J., Hunter A., Cole T. The importance of differentiating Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromes. J Med Genet. 1992 Dec;29(12):928–928. doi: 10.1136/jmg.29.12.928-b. [DOI] [PMC free article] [PubMed] [Google Scholar]
Xuan J. Y., Besner A., Ireland M., Hughes-Benzie R. M., MacKenzie A. E. Mapping of Simpson-Golabi-Behmel syndrome to Xq25-q27. Hum Mol Genet. 1994 Jan;3(1):133–137. doi: 10.1093/hmg/3.1.133. [DOI] [PubMed] [Google Scholar]

ACTIONS

RESOURCES