Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1992 Jan;29(1):56–57. doi: 10.1136/jmg.29.1.56

Exclusion of calcitonin/alpha-CGRP gene defect in a family with autosomal dominant supravalvular aortic stenosis.

G M Pastores 1, V V Michels 1, D J Schaid 1, D J Driscoll 1, R H Feldt 1, S N Thibodeau 1
PMCID: PMC1015824  PMID: 1552547

Full text

PDF
56

Selected References

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

  1. Bennett C. P., Burn J., Moore G. E., Chambers J., Williamson R., Wilkinson J. Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosis. J Med Genet. 1988 May;25(5):311–312. doi: 10.1136/jmg.25.5.311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Broad P. M., Symes A. J., Thakker R. V., Craig R. K. Structure and methylation of the human calcitonin/alpha-CGRP gene. Nucleic Acids Res. 1989 Sep 12;17(17):6999–7011. doi: 10.1093/nar/17.17.6999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Culler F. L., Jones K. L., Deftos L. J. Imparied calcitonin secretion in patients with Williams syndrome. J Pediatr. 1985 Nov;107(5):720–723. doi: 10.1016/s0022-3476(85)80399-1. [DOI] [PubMed] [Google Scholar]
  4. Hitman G. A., Garde L., Daoud W., Snodgrass G. J. The calcitonin-CGRP gene in the infantile hypercalcaemia/Williams-Beuren syndrome. J Med Genet. 1989 Oct;26(10):609–613. doi: 10.1136/jmg.26.10.609. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Lathrop G. M., Lalouel J. M. Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet. 1984 Mar;36(2):460–465. [PMC free article] [PubMed] [Google Scholar]
  6. Russo A. F., Chamany K., Klemish S. W., Hall T. M., Murray J. C. Characterization of the calcitonin/CGRP gene in Williams syndrome. Am J Med Genet. 1991 Apr 1;39(1):28–33. doi: 10.1002/ajmg.1320390108. [DOI] [PubMed] [Google Scholar]
  7. Schmidt M. A., Ensing G. J., Michels V. V., Carter G. A., Hagler D. J., Feldt R. H. Autosomal dominant supravalvular aortic stenosis: large three-generation family. Am J Med Genet. 1989 Mar;32(3):384–389. doi: 10.1002/ajmg.1320320324. [DOI] [PubMed] [Google Scholar]
  8. Thibodeau S. N., Dorkins H. R., Faulk K. R., Berry R., Smith A. C., Hagerman R., King A., Davies K. E. Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome. Hum Genet. 1988 Jul;79(3):219–227. doi: 10.1007/BF00366240. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES