-
1
-
-
0026011654
-
Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction
-
Mancuso D.J., Tuley E.A., Westfield L.A., Teresa L., Mancuso L., Michelle M., et al. Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction. Biochemistry 1991, 30:253-269.
-
(1991)
Biochemistry
, vol.30
, pp. 253-269
-
-
Mancuso, D.J.1
Tuley, E.A.2
Westfield, L.A.3
Teresa, L.4
Mancuso, L.5
Michelle, M.6
-
2
-
-
0024331438
-
Structure of gene for human von Willebrand factor
-
Mancuso D.J., Tuley E.A., Westfield L.A., Wornall N.K., Shelton-Inloes B., Sorace J.M., et al. Structure of gene for human von Willebrand factor. J Biol Chem 1989, 264:19814-19827.
-
(1989)
J Biol Chem
, vol.264
, pp. 19814-19827
-
-
Mancuso, D.J.1
Tuley, E.A.2
Westfield, L.A.3
Wornall, N.K.4
Shelton-Inloes, B.5
Sorace, J.M.6
-
3
-
-
77649182633
-
-
http://www.vwf.group.shef.ac.uk.
-
-
-
-
4
-
-
0027472182
-
A database of polymorphisms in the von Willebrand factor gene and pseudogene. For the Consortium on von Willebrand Factor Mutations and Polymorphisms and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
-
Sadler J.E., Ginsburg D. A database of polymorphisms in the von Willebrand factor gene and pseudogene. For the Consortium on von Willebrand Factor Mutations and Polymorphisms and the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 1993, 69:185-191.
-
(1993)
Thromb Haemost
, vol.69
, pp. 185-191
-
-
Sadler, J.E.1
Ginsburg, D.2
-
5
-
-
77649190868
-
-
NW_001838735.2|Hs22_WGA1294_36 (based on HuRef SCAF_1103279180335).
-
NW_001838735.2|Hs22_WGA1294_36 (based on HuRef SCAF_1103279180335). http://blast.ncbi.nlm.nih.gov/Blast.cgi.
-
-
-
-
6
-
-
0026640029
-
Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I
-
Zhang Z.P., Lindstedt M., Falk G., Blomback M., Egberg M.N., Anvret M. Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I. Am J Hum Genet 1992, 51:850-858.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 850-858
-
-
Zhang, Z.P.1
Lindstedt, M.2
Falk, G.3
Blomback, M.4
Egberg, M.N.5
Anvret, M.6
-
7
-
-
0028321794
-
Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin
-
Zhang Z.P., Blomback M., Egberg N., Falk G., Anvret M. Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin. Genomics 1994, 21:188-193.
-
(1994)
Genomics
, vol.21
, pp. 188-193
-
-
Zhang, Z.P.1
Blomback, M.2
Egberg, N.3
Falk, G.4
Anvret, M.5
-
8
-
-
48749111184
-
Genetic defects in von Willebrand disease type 3 in Indian and Greek patients
-
Gupta P.K., Saxena R., Adamtziki E., Budde U., Oyen F., Obser T., et al. Genetic defects in von Willebrand disease type 3 in Indian and Greek patients. Blood Cells Mol Dis 2008, 41:219-222.
-
(2008)
Blood Cells Mol Dis
, vol.41
, pp. 219-222
-
-
Gupta, P.K.1
Saxena, R.2
Adamtziki, E.3
Budde, U.4
Oyen, F.5
Obser, T.6
-
9
-
-
0033782679
-
Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease
-
Baronciani L., Cozzi G., Canciani M.T., Peyvandi F., Srivastava A., Federici A.B., et al. Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease. Thromb Haemost 2000, 84:536-540.
-
(2000)
Thromb Haemost
, vol.84
, pp. 536-540
-
-
Baronciani, L.1
Cozzi, G.2
Canciani, M.T.3
Peyvandi, F.4
Srivastava, A.5
Federici, A.B.6
-
10
-
-
62549143505
-
Rapid molecular diagnosis of von Willebrand disease by direct sequencing. Detection of 12 novel putative mutations in VWF gene
-
Corrales I., Ramirez L., Altisent C., Parra R., Vidal F. Rapid molecular diagnosis of von Willebrand disease by direct sequencing. Detection of 12 novel putative mutations in VWF gene. Thromb Haemost 2009, 101:570-576.
-
(2009)
Thromb Haemost
, vol.101
, pp. 570-576
-
-
Corrales, I.1
Ramirez, L.2
Altisent, C.3
Parra, R.4
Vidal, F.5
-
11
-
-
0031957351
-
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin
-
Eikenboom J.C., Castaman G., Vos H.L., Bertina R.M., Rodeghiero F. Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin. Thromb Haemost 1998, 79:709-717.
-
(1998)
Thromb Haemost
, vol.79
, pp. 709-717
-
-
Eikenboom, J.C.1
Castaman, G.2
Vos, H.L.3
Bertina, R.M.4
Rodeghiero, F.5
-
12
-
-
0029658166
-
A novel mutation Gly?1672 Arg in type 2A and a homozygous mutation in type 2B von Willebrand Disease
-
Hagiwara T., Inaba H., Yoshida S., Nagaizumi K., Arai M., Hanabusa H., et al. A novel mutation Gly?1672 Arg in type 2A and a homozygous mutation in type 2B von Willebrand Disease. Thromb Haemost 1996, 76:253-257.
-
(1996)
Thromb Haemost
, vol.76
, pp. 253-257
-
-
Hagiwara, T.1
Inaba, H.2
Yoshida, S.3
Nagaizumi, K.4
Arai, M.5
Hanabusa, H.6
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