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Thromb Haemost 2000; 84(02): 351-352
DOI: 10.1055/s-0037-1614020
DOI: 10.1055/s-0037-1614020
Letters to the Editor
Pregnancy in Women with Type 1 von Willebrand Disease Caused by Heterozygosity for von Willebrand Factor Mutation C1130F
Authors
Further Information
Publication History
Received
19 April 2000
Accepted
20 April 2000
Publication Date:
14 December 2017 (online)
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References
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- 2 Castaman G, Eikenboom JCJ, Missiaglia E, Rodeghiero F. Autosomal dominant type 1 von Willebrand disease due to G3639T mutation (C1130F) in exon 26 of von Willebrand factor gene: description of five Italian families and evidence for a founder effect. Br I Haematol 2000; 108: 876-9.
- 3 Conti M, Mari D, Conti E, Muggiasca ML, Mannucci PM. Pregnancy in women with different types of von Willebrand disease. Obstet Gynecol 1986; 68: 282-5.
- 4 Greer IA, Lowe GD, Walker II, Forbes CD. Haemorrhagic problems in obstetrics and gynaecology in patients with congenital coagulopathies. Br I Obstet Gynaecol 1991; 98: 909-18.
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- 6 Castaman G, Rodeghiero F. Cunrent management of von Willebrand’s disease. Drugs 1995; 50: 602-12.
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