Peake I.R.,1990
Peake I.R., Liddell M.B., Moodie P., Standen G., Mancuso D.J., Tuley E.A., Westfield L.A., Sorace J.M., Sadler J.E., Verweij C.L., Bloom A. Severe Type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene:family studies that identify carriers of the condition and a compound heterozygous individual. - Blood, 1990, v. 75, p. 654-661.
