Pietu G.,1992


Pietu G., Ribba A.S. de Paillette L., Cherel G., Lavergne J.M., Bahnak B.R., Meyer D. Molecular study of von Willebrand disease: identification of potential mutations in patients with type IIA and type IIB. - Blood Coagul.Fibrinolysis, 1992, v.3, p. 415-421.

Смотрите также:

  • Табл. W mut