Zhang Z.P.,1992b
Zhang Z.P., Falk G., Blomback M., Egberg N., Anvret M. A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients. - Hum.Mol.Genet., 1992, v. 1, p. 767-768.
Zhang Z.P., Falk G., Blomback M., Egberg N., Anvret M. A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients. - Hum.Mol.Genet., 1992, v. 1, p. 767-768.
