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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group. Cell. 1993 Mar 26;72(6):971–983. doi: 10.1016/0092-8674(93)90585-e. [DOI] [PubMed] [Google Scholar]
- Collins F. S. Of needles and haystacks: finding human disease genes by positional cloning. Clin Res. 1991 Dec;39(4):615–623. [PubMed] [Google Scholar]
- Germino G. G., Somlo S. A positional cloning approach to inherited renal disease. Semin Nephrol. 1992 Nov;12(6):541–553. [PubMed] [Google Scholar]
- Reeders S. T., Breuning M. H., Davies K. E., Nicholls R. D., Jarman A. P., Higgs D. R., Pearson P. L., Weatherall D. J. A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16. Nature. 1985 Oct 10;317(6037):542–544. doi: 10.1038/317542a0. [DOI] [PubMed] [Google Scholar]
- Scheinman S. J., Pook M. A., Wooding C., Pang J. T., Frymoyer P. A., Thakker R. V. Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies. J Clin Invest. 1993 Jun;91(6):2351–2357. doi: 10.1172/JCI116467. [DOI] [PMC free article] [PubMed] [Google Scholar]
