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Research Article

PLATELET RELEASE DEFECT IN A CHILD WITH EHLERS-DANLOS SYNDROME

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Pages 193-194 | Published online: 09 Jul 2009

REFERENCES

  • Beylot C, Bioulac P. Le syndrome d'Ehlers—Danlos. Bordeaux Med. 1978;11:115–128.
  • McKusick VA, Pyeritz RE. Heritable and developmetal disorders of connective tissues and bone. In: McCarty DJ, ed. Arthritis and Allied Conditions, Vol 1. Philadelphia: Lea 8c Febiger; 1985:1168–1194.
  • Sasaki T, Arai K, Ono M, Yamaguchi T, Furuta S, Nagai Y Ehlers—Danlos syndrome: a varient charac-terized by the deficiency of pro alpha 2 chain of type I procollagen. Arch Dermatol. 1987;123:76–79.
  • Beighton P, de Paepe A, Danks D, et al. International nosolgy of heritable disorders of connective tissue: Berlin. AmJ Med Genetic 1986;29:581–594.
  • Anstey A, Mayne K, Winter M, de Pette JV, Popes FM. Platelet and coagulation studies in Ehlers—Danlos syndrome. BrJDermatol. 1991;125:155–163.

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