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Journal Articles

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

NJ Beauchamp, ME Daly, PC Cooper, M Makris, FE Preston, IR Peake

Blood (1996) 88 (5): 1700–1707.

https://doi.org/10.1182/blood.V88.5.1700.1700

Published: 1996

Journal Articles

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

EW Murray, AR Giles, PJ Bridge, IR Peake, DP Lillicrap

Blood (1991) 77 (7): 1476–1483.

https://doi.org/10.1182/blood.V77.7.1476.1476

Published: 1991

Journal Articles

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, MB Liddell, JE Sadler, G Standen, AL Bloom

Blood (1990) 76 (3): 555–561.

https://doi.org/10.1182/blood.V76.3.555.555

Published: 1990

Journal Articles

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, P Moodie, G Standen, DJ Mancuso, EA Tuley, LA Westfield, JM Sorace, JE Sadler, CL Verweij

Blood (1990) 75 (3): 654–661.

https://doi.org/10.1182/blood.V75.3.654.654

Published: 1990