Prevalence of Protein C Deficiency in the Healthy Population

Robert C. Tait, Isobel D. Walker, P H Reitsma, +5

Thrombosis and Haemostasis

NutritionGeneticsGenetic EpidemiologyHuman PolymorphismPathology +18

Protein C Deficiency: A Database of Mutations, 1995 Update

P H Reitsma, Francesca Bernardi, Rowan G. Doig, +11

Thrombosis and Haemostasis

Protein C DeficiencyGenetic DisorderGeneticsPathogenesisPathology +4

Factor XIII Val34Leu Is a Genetic Factor Involved in the Aetiology of Venous Thrombosis

P H Reitsma, Dayse Maria Lourenço, Francisco Humberto de Abreu Maffei, +6

Thrombosis and Haemostasis

Deep Venous ThrombosisGeneticsImmunologyHuman PolymorphismPathology +20

Disruption of a binding site for hepatocyte nuclear factor 4 results in hemophilia B Leyden.

M J Reijnen, Frances M. Sladek, R M Bertina, +1

Proceedings of the National Academy of Sciences

GeneticsPathologyHemophilia B LeydenRedox BiologyTranscriptional Regulation +14

Haemophilia B: database of point mutations and short additions and deletions, fifth edition, 1994

F. Giannelli, P.M. Green, Steve S. Sommer, +7

Nucleic Acids Research

Haemophilia B: database of point mutations and short additions and deletions—fourth edition, 1993

F. Giannelli, P.M. Green, Katherine A. High, +8

Nucleic Acids Research

Protein C deficiency: summary of the 1995 database update

P H Reitsma

Nucleic Acids Research

ImmunologyPathologyDisease Gene IdentificationProtein GeneticsThrombosis +17

Identification of Eight Point Mutations in Protein S Deficiency Type I – Analysis of 15 Pedigrees

P H Reitsma, E. Gómez, S R Poort, +1

Thrombosis and Haemostasis

Mendelian DisorderPoint MutationsEight Point MutationsMedicineGenetics +12

Biogenesis of Weibel-Palade bodies in von Willebrand's disease variants with impaired von Willebrand factor intrachain or interchain disulfide bond formation

Jiong‐Wei Wang, Dafna J. Groeneveld, Gwenny Cosemans, +5

Haematologica

Twelve novel and two recurrent mutations in 14 Austrian families with hereditary protein C deficiency

S R Poort, Ingrid Pabinger-Fasching, Christine Mannhalter, +2

Blood Coagulation & Fibrinolysis

Family MembersGeneticsMolecular BiologyPathologyMolecular Genetics +14