IR Peake

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 et al. · Blood · 1990 · 159 citations

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 et al. · Blood · 1990 · 71 citations · Full text

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

N Beauchamp, ME Daly, P. Cooper et al. · Blood · 1996 · 33 citations · Full text

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

N Beauchamp, ME Daly, P. Cooper et al. · Blood · 1996 · 25 citations · Full text

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

AR Giles, PJ Bridge, IR Peake et al. · Blood · 1991 · 14 citations · Full text