tryptophan and Deficiency, Factor II

tryptophan has been researched along with Deficiency, Factor II in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bertina, RM; Landolfi, R; Poort, SR	1
Augustine, J; Rappaport, EF; Schwartz, E; Shalmon, L; Surrey, S; Tamary, H	1

Other Studies

2 other study(ies) available for tryptophan and Deficiency, Factor II

Article	Year
Compound heterozygosity for two novel missense mutations in the prothrombin gene in a patient with a severe bleeding tendency. Thrombosis and haemostasis, 1997, Volume: 77, Issue:4 Topics: Blood Coagulation Factors; Cysteine; Female; Genetic Predisposition to Disease; Genetic Variation; Hemorrhage; Heterozygote; Humans; Hypoprothrombinemias; Infant, Newborn; Point Mutation; Prothrombin; Reference Values; Sequence Analysis, DNA; Tryptophan; Tyrosine	1997
Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP). Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1997, Volume: 8, Issue:6 Topics: Adult; Arginine; Codon; Computer Simulation; Female; Frameshift Mutation; Gene Deletion; Heterozygote; Humans; Hypoprothrombinemias; Models, Molecular; Polymerase Chain Reaction; Prothrombin; Sequence Analysis, DNA; Thrombin; Tryptophan	1997

Article

Year

Compound heterozygosity for two novel missense mutations in the prothrombin gene in a patient with a severe bleeding tendency.

Thrombosis and haemostasis, 1997, Volume: 77, Issue:4

Topics: Blood Coagulation Factors; Cysteine; Female; Genetic Predisposition to Disease; Genetic Variation; Hemorrhage; Heterozygote; Humans; Hypoprothrombinemias; Infant, Newborn; Point Mutation; Prothrombin; Reference Values; Sequence Analysis, DNA; Tryptophan; Tyrosine

1997

Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP).

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis, 1997, Volume: 8, Issue:6

Topics: Adult; Arginine; Codon; Computer Simulation; Female; Frameshift Mutation; Gene Deletion; Heterozygote; Humans; Hypoprothrombinemias; Models, Molecular; Polymerase Chain Reaction; Prothrombin; Sequence Analysis, DNA; Thrombin; Tryptophan

1997