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pro vyhledávání: '"Anthony M. Cumming"'
Autor:
Charles R. M. Hay, Paula H B Bolton-Maggs, Gillian N Pike, Jecko Thachil, John Burthem, Anthony M Cumming
Publikováno v:
Blood. 124:696-696
Introduction: FXI deficiency is characterised by a variable bleeding tendency. No clear correlation exists between bleeding and either FXI:C level or genotype. Some patients with major FXI deficiency (FXI:C Aims: To identify the optimal TG assay cond
Autor:
Megan Sutherland, Jecko Thachil, John Burthem, Brenda Sempasa, Paula H B Bolton-Maggs, Gillian N Pike, Anthony M Cumming, Charles R. M. Hay
Publikováno v:
Blood. 124:1519-1519
Introduction: Factor XI (FXI) deficiency is an autosomally inherited bleeding disorder characterised by an increased risk of excessive bleeding following trauma or surgery. However, considerable phenotypic heterogeneity of the bleeding tendency is ob
Publikováno v:
Human genetics. 89(2)
We have used the polymerase chain reaction to amplify two variable number of tandem repeats (VNTRs) within a region of repetitive DNA located in intron 40 of the von Willebrand factor (vWf) gene. Heterozygosity for VNTR I was observed in 30 out of 39