Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene

IR Peake, D. Bowen, P Bignell, +4

Blood

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

IR Peake, MB Liddell, Peter Moodie, +7

Blood

Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V leiden

N Beauchamp, ME Daly, P. Cooper, +3

Blood

Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V leiden

N Beauchamp, ME Daly, P. Cooper, +3

Blood

Cosegregation of von Willebrand factor gene polymorphisms and possible germinal mosaicism in type IIB von Willebrand disease

AR Giles, PJ Bridge, IR Peake, +1

Blood