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Molecular analysis of the genotype-phenotype relationship in factor X deficiency.
Published in:
Human Genetics, 2000, v. 106, n. 2, p. 249, doi. 10.1007/s004390051035
By:
- Millar, David S.;
- Elliston, Lyn;
- Deex, Pippa;
- Krawczak, Michael;
- Wacey, Adam I.;
- Reynaud, Jacqueline;
- Nieuwenhuis, H. Karel;
- Bolton-Maggs, Paula;
- Mannucci, Pier M.;
- Reverter, Joan Carlos;
- Cachia, Phillip;
- Pasi, K. John;
- Layton, D. Mark;
- Cooper, David N.
Publication type:
Article
The Factor VIII Structure and Mutation Resource Site: HAMSTeRS Version 4.
Published in:
Nucleic Acids Research, 1998, v. 26, n. 1, p. 218
By:
- Kemball‐Cook, Geoffrey;
- Tuddenham, Edward G. D.;
- Wacey, Adam I.
Publication type:
Article
The Haemophilia A Mutation Search Test and Resource Site, Home Page of the Factor VIII Mutation Database: HAMSTeRS.
Published in:
Nucleic Acids Research, 1996, v. 24, n. 1, p. 100, doi. 10.1093/nar/24.1.100
By:
- Wacey, Adam I.;
- Kemball-Cook, Geoffrey;
- Kazazian, Haig H.;
- Antonarakis, Stylianos E.;
- Schwaab, Rainer;
- Lindley, Peter;
- Tuddenham, E. G. D.
Publication type:
Article
Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII.
Published in:
British Journal of Haematology, 1994, v. 86, n. 3, p. 610, doi. 10.1111/j.1365-2141.1994.tb04793.x
By:
- Bernardi, F.;
- Liney, D. L.;
- Patracchini, P.;
- Gemmati, D.;
- Legnani, C.;
- Arcieri, P.;
- Pinotti, M.;
- Redaelli, R.;
- Ballerini, G.;
- Pemberton, S.;
- Wacey, A. I.;
- Mariani, G.;
- Tuddenham, E. G. D.;
- Marchetti, G.
Publication type:
Article
A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiency.
Published in:
British Journal of Haematology, 1993, v. 84, n. 2, p. 290, doi. 10.1111/j.1365-2141.1993.tb03067.x
By:
- Wacey, A. I.;
- Pemberton, S.;
- Cooper, D. N.;
- Kakkar, V. V.;
- Tuddenham, E. G. D.
Publication type:
Article

Found: 5

Molecular analysis of the genotype-phenotype relationship in factor X deficiency.

The Factor VIII Structure and Mutation Resource Site: HAMSTeRS Version 4.

The Haemophilia A Mutation Search Test and Resource Site, Home Page of the Factor VIII Mutation Database: HAMSTeRS.

Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII.

A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiency.