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J R Soc Med. 1990 August; 83(8): 531–532.
PMCID: PMC1292786

Familial Raynaud's phenomenon and localized scleroderma associated with essential telangiectasia and cytogenetic abnormalities.

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Selected References

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  • Sherer GK, Jackson BB, Leroy EC. Chromosome breakage and sister chromatid exchange frequencies in scleroderma. Arthritis Rheum. 1981 Nov;24(11):1409–1413. [PubMed]
  • Wuthrich RC, Roenigk HH, Steck WD. Localized scleroderma. Arch Dermatol. 1975 Jan;111(1):98–100. [PubMed]
  • Sasaki S, Yoshino H. Systemic scleroderma in mother and daughter. Arch Dermatol. 1977 Mar;113(3):378–379. [PubMed]
  • Wolff S. Sister chromatid exchange. Annu Rev Genet. 1977;11:183–201. [PubMed]
  • Krieg T, Meurer M. Systemic scleroderma. Clinical and pathophysiologic aspects. J Am Acad Dermatol. 1988 Mar;18(3):457–481. [PubMed]

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