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A C Fitches

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Thrombosis and Haemostasis|November 1, 2001

Creation of an additional glycosylation site as a mechanism for type I antithrombin deficiencyA C Fitches, K Lewandowski, R J Olds

British Journal of Haematology|July 11, 2000

The multigenic basis for venous thrombosisR J Olds, A C Fitches, C P Geary

Pathology|November 1, 1996

A novel antithrombin gene mutation: slippage and mispairing as a mechanism of genetic diseaseA C Fitches, S J May, R J Olds

Human Genetics|December 1, 1992

Analysis of beta-globin gene haplotypes in Asian Indians: origin and spread of beta-thalassaemia on the Indian subcontinentN Y Varawalla, A C Fitches, J M Old

Blood|December 9, 1998

Impaired cotranslational processing as a mechanism for type I antithrombin deficiencyA C Fitches, R Appleby, D A Lane, et al.

Blood|June 11, 1999

Familial overexpression of beta antithrombin caused by an Asn135Thr substitutionT A Bayston, A Tripodi, P M Mannucci, et al.

Thrombosis and Haemostasis|January 1, 1997

Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisD A Lane, T Bayston, R J Olds, et al.

Pageof 1

Search research articles

Showing results (1-10 of 7) with videos related to

Sort By:

Pageof 1

Thrombosis and Haemostasis|November 1, 2001

Creation of an additional glycosylation site as a mechanism for type I antithrombin deficiencyA C Fitches, K Lewandowski, R J Olds

British Journal of Haematology|July 11, 2000

The multigenic basis for venous thrombosisR J Olds, A C Fitches, C P Geary

Pathology|November 1, 1996

A novel antithrombin gene mutation: slippage and mispairing as a mechanism of genetic diseaseA C Fitches, S J May, R J Olds

Human Genetics|December 1, 1992

Analysis of beta-globin gene haplotypes in Asian Indians: origin and spread of beta-thalassaemia on the Indian subcontinentN Y Varawalla, A C Fitches, J M Old

Blood|December 9, 1998

Impaired cotranslational processing as a mechanism for type I antithrombin deficiencyA C Fitches, R Appleby, D A Lane, et al.

Blood|June 11, 1999

Familial overexpression of beta antithrombin caused by an Asn135Thr substitutionT A Bayston, A Tripodi, P M Mannucci, et al.

Thrombosis and Haemostasis|January 1, 1997

Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and HaemostasisD A Lane, T Bayston, R J Olds, et al.

Pageof 1