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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