Inbal A.,1992

Inbal A., Seligsohn U., Kornbrot N., Brenner B., Harrison P., Randi A., Rabinowitz I., Sadler J.E. Characterization of three mutations causing von Willebrand disease type IIA in five unrelated families. - Thromb.Haemost., 1992, v. 67, p. 618-622.

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