126 related articles for article (PubMed ID: 1674891)
21. Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type III.
Zhang ZP; Falk G; Blombäck M; Egberg N; Anvret M
Hum Mol Genet; 1992 Apr; 1(1):61-2. PubMed ID: 1301136
[No Abstract] [Full Text] [Related]
22. The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain.
Cooney KA; Nichols WC; Bruck ME; Bahou WF; Shapiro AD; Bowie EJ; Gralnick HR; Ginsburg D
J Clin Invest; 1991 Apr; 87(4):1227-33. PubMed ID: 1672694
[TBL] [Abstract][Full Text] [Related]
23. Characterisation of 98 alleles in 105 unrelated individuals in the F8VWF gene.
Mercier B; Gaucher C; Mazurier C
Nucleic Acids Res; 1991 Sep; 19(17):4800. PubMed ID: 1679932
[No Abstract] [Full Text] [Related]
24. Von Willebrand factor 1 and factor 2 alleles (intron 40) are suitable markers for carrier detection in von Willebrand disease families in the Indian population.
Trasi S; Mohanty D; Pathare A; Shetty S; Ghosh K
Acta Haematol; 2006; 115(1-2):64-7. PubMed ID: 16424652
[TBL] [Abstract][Full Text] [Related]
25. [Detection of gene mutation and genetic analysis of a patient with type 3 von Willebrand disease].
Li Z; Wang Y; Wan H
Zhonghua Xue Ye Xue Za Zhi; 1998 Mar; 19(3):122-4. PubMed ID: 11243141
[TBL] [Abstract][Full Text] [Related]
26. von Willebrand disease masquerading as haemophilia A.
Mazurier C
Thromb Haemost; 1992 Apr; 67(4):391-6. PubMed ID: 1631785
[No Abstract] [Full Text] [Related]
27. [Molecular biology of blood coagulation disorders].
Saito H
Nihon Naika Gakkai Zasshi; 1991 Oct; 80(10):1682-6. PubMed ID: 1685509
[No Abstract] [Full Text] [Related]
28. Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I.
Zhang ZP; Lindstedt M; Falk G; Blombäck M; Egberg N; Anvret M
Am J Hum Genet; 1992 Oct; 51(4):850-8. PubMed ID: 1415226
[TBL] [Abstract][Full Text] [Related]
29. Impact of 789Ala/Ala genotype on quantitative type of von Willebrand disease.
Ahmad F; Kannan M; Biswas A; Saxena R
Ann Hematol; 2009 May; 88(5):479-83. PubMed ID: 18923835
[TBL] [Abstract][Full Text] [Related]
30. Challenges in diagnosis of von Willebrand disease in the presence of combined mutations of different genes.
Nava T; Dubé E; Gauthier J; Vézina C; Bonnefoy A; Lillicrap D; Rivard GE
Haemophilia; 2019 Mar; 25(2):e113-e117. PubMed ID: 30690834
[No Abstract] [Full Text] [Related]
31. Discordant von Willebrand factor (VWF) activity in patients with VWF p.Gly1324Ser confirmed in vitro.
Bowman M; Rimmer E; Houston DS; Israels SJ; James P
Haemophilia; 2018 Mar; 24(2):e57-e59. PubMed ID: 29341351
[No Abstract] [Full Text] [Related]
32. Practical application of three polymorphic microsatellites in intron 40 of the human von Willebrand factor gene.
Casaña P; Martinez F; Aznar JA; Lorenzo JI; Jorquera JI
Haemostasis; 1995; 25(6):264-71. PubMed ID: 8586316
[TBL] [Abstract][Full Text] [Related]
33. Genetic linkage of two intragenic restriction fragment length polymorphisms with von Willebrand's disease type IIA. Evidence for a defect in the von Willebrand factor gene.
Verweij CL; Quadt R; Briët E; Dubbeldam K; van Ommen GB; Pannekoek H
J Clin Invest; 1988 Apr; 81(4):1116-21. PubMed ID: 2895123
[TBL] [Abstract][Full Text] [Related]
34. Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population.
Kasatkar P; Ghosh K; Shetty S
Indian J Med Res; 2015 Dec; 142(6):759-62. PubMed ID: 26831425
[No Abstract] [Full Text] [Related]
35. Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction.
Mancuso DJ; Tuley EA; Westfield LA; Lester-Mancuso TL; Le Beau MM; Sorace JM; Sadler JE
Biochemistry; 1991 Jan; 30(1):253-69. PubMed ID: 1988024
[TBL] [Abstract][Full Text] [Related]
36. Instability of a variable number tandem repeat in intron 40 of the human von Willebrand factor gene.
Casaña P; Martinez F; Aznar JA
Br J Haematol; 1995 Sep; 91(1):255-6. PubMed ID: 7577646
[No Abstract] [Full Text] [Related]
37. [Importance of the study of the binding of factor VIII to von Willebrand factor in hemophilia A].
Batlle J; Blanco-López MJ; Castiñeira MP; López-Fernández MF
Sangre (Barc); 1992 Jun; 37(3):211-24. PubMed ID: 1359656
[No Abstract] [Full Text] [Related]
38. Biology of inherited coagulopathies: von Willebrand factor.
Ginsburg D
Hematol Oncol Clin North Am; 1992 Oct; 6(5):1011-20. PubMed ID: 1400069
[TBL] [Abstract][Full Text] [Related]
39. Molecular genetic analysis of porcine von Willebrand disease: tight linkage to the von Willebrand factor locus.
Bahou WF; Bowie EJ; Fass DN; Ginsburg D
Blood; 1988 Jul; 72(1):308-13. PubMed ID: 2898953
[TBL] [Abstract][Full Text] [Related]
40. A novel case of compound heterozygosity with "Normandy"/type I von Willebrand disease (vWD). Direct demonstration of the segregation of one allele with a defective expression at the mRNA level causing type I vWD.
Siguret V; Lavergne JM; Chérel G; Boyer-Neumann C; Ribba AS; Bahnak BR; Meyer D; Piétu G
Hum Genet; 1994 Feb; 93(2):95-102. PubMed ID: 7906671
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
