Abstract
Although cystic fibrosis (CF) is among the most common inherited diseases in Caucasian populations1, the basic biochemical defect is not yet known. CF is inherited as an autosomal recessive trait apparently due to mutations in a single gene2–4, whence the efforts made to identify the genetic locus responsible by linkage studies. Two markers have recently been identified that are genetically linked to CF: one is a genetic variation in serum level of activity of the enzyme paraoxonase5, and the other is a restriction fragment length polymorphism (RFLP) identified with a randomly isolated DNA probe4. We report here that the genetic locus DOCRI-917 defined by the cloned DNA probe is located on chromosome 7.
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References
Talamo, R. C., Rosenstein, B. J. & Berninger, R. W. in The Metabolic Basis of Inherited Disease 5th edn (eds Stanbury, J. B. et al.) 1889–1917 (McGraw-Hill, New York, 1983).
Danks, D. M., Phelan, P. D. & Chapman, C. Am. J. hum. Genet. 36, 1389–1402 (1984).
Romeo, G. et al. Am. J. hum. Genet. 37, 338–349 (1985).
Tsui, L.-C. et al. Science (in the press).
Schmiegelow, K. et al. Lancet (in the press).
Lawn, R. M., Fritsch, E. F., Parker, R. C., Blake, G. & Maniatis, T. Cell 15, 1157–1174 (1978).
Schumm, J. W. et al. 8th Human Gene Mapping Workshop, Helsinki (1985); Cytogenet. Cell Genet. (in the press).
Botstein, D., White, R. L., Skolnick, M. & Davis, R. W. Am. J. hum. Genet. 32, 314–331 (1980).
Van Cong, Nguyen, Weil, D. & Finaz, C. Annls Génét (in the press).
Grzeschik, K. H. Somatic Cell Genet. 2, 401–410 (1976).
Jones, N. et al. Science 227, 311–314 (1985).
Barker, P. E., Ruddle, F. H., Royer, H.-D., Acuto, O. & Reinherz, E. L. Science 226, 348–349 (1984).
Collins, M. K. L. et al. EMBO J. 3, 2347–2349 (1984).
Isobe, M., Erikson, J., Emanuel, B. S., Nowell, P. C. & Croce, C. Science 228, 580–582.(1985).
Morton, C. C., Duby, A. D., Eddy, R. L., Shows, T. B. & Seidman, J. G. Science 228, 582–584 (1985).
Shows, T. B. Biochem. Genet. 7, 193–204 (1972).
Gedde-Dahl, T. et al. 8th Human Gene Mapping Workshop, Helsinki (1985); Cytogenet. Cell Genet. (in the press).
Meera Khan, P. & Robson, E. B. Human Gene Mapping 5, 39–46 (1979).
Wahl, G. M., Stern, M. & Stark, G. R. Proc. natn. Acad. Sci. U.S.A. 75, 3683–3687 (1979).
Gross, M.-S. et al. Annls Génét. 25, 87–91 (1982).
Weil, D. et al. Annls Génét. 24, 89–92 (1981).
Retief, E., Parker, M. I. & Retief, A. E. Hum. Genet. 69, 304–308 (1985).
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Knowlton, R., Cohen-Haguenauer, O., Van Cong, N. et al. A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7. Nature 318, 380–382 (1985). https://doi.org/10.1038/318380a0
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DOI: https://doi.org/10.1038/318380a0
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