K. Chapman, M. Seldon, R. Richards: Thrombotic microangiopathies, thrombotic thrombocytopenic purpura, and ADAMTS-13. Seminars in Thrombosis and Hemostasis, 2012, 38. vsk, nro 1, s. 47–54. PubMed:22314603. doi:10.1055/s-0031-1300951. ISSN 0094-6176. Artikkelin verkkoversio. (englanniksi)
P. D. James, D. Lillicrap: The molecular characterization of von Willebrand disease: good in parts. British journal of haematology, 2013, 161. vsk, nro 2, s. 166–176. PubMed:23406206. doi:10.1111/bjh.12249. ISSN 0007-1048. Artikkelin verkkoversio. (englanniksi)
J. M. Johnsen et al: Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project. Blood, 2013, 122. vsk, nro 4, s. 590–597. PubMed:23690449. doi:10.1182/blood-2013-02-485094. ISSN 0006-4971. Artikkelin verkkoversio. (englanniksi)
L. Baronciani, A. Goodeve, F. Peyvandi: Molecular diagnosis of von Willebrand disease. Haemophilia, 2017, 23. vsk, nro 2, s. 188–197. doi:10.1111/hae.13175. Artikkelin verkkoversio. (englanniksi)
K. Chapman, M. Seldon, R. Richards: Thrombotic microangiopathies, thrombotic thrombocytopenic purpura, and ADAMTS-13. Seminars in Thrombosis and Hemostasis, 2012, 38. vsk, nro 1, s. 47–54. PubMed:22314603. doi:10.1055/s-0031-1300951. ISSN 0094-6176. Artikkelin verkkoversio. (englanniksi)
P. D. James, D. Lillicrap: The molecular characterization of von Willebrand disease: good in parts. British journal of haematology, 2013, 161. vsk, nro 2, s. 166–176. PubMed:23406206. doi:10.1111/bjh.12249. ISSN 0007-1048. Artikkelin verkkoversio. (englanniksi)
J. M. Johnsen et al: Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project. Blood, 2013, 122. vsk, nro 4, s. 590–597. PubMed:23690449. doi:10.1182/blood-2013-02-485094. ISSN 0006-4971. Artikkelin verkkoversio. (englanniksi)
P. D. James, D. Lillicrap: The molecular characterization of von Willebrand disease: good in parts. British journal of haematology, 2013, 161. vsk, nro 2, s. 166–176. PubMed:23406206. doi:10.1111/bjh.12249. ISSN 0007-1048. Artikkelin verkkoversio. (englanniksi)
J. M. Johnsen et al: Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project. Blood, 2013, 122. vsk, nro 4, s. 590–597. PubMed:23690449. doi:10.1182/blood-2013-02-485094. ISSN 0006-4971. Artikkelin verkkoversio. (englanniksi)
L. Baronciani, A. Goodeve, F. Peyvandi: Molecular diagnosis of von Willebrand disease. Haemophilia, 2017, 23. vsk, nro 2, s. 188–197. doi:10.1111/hae.13175. Artikkelin verkkoversio. (englanniksi)
thieme-connect.de
K. Chapman, M. Seldon, R. Richards: Thrombotic microangiopathies, thrombotic thrombocytopenic purpura, and ADAMTS-13. Seminars in Thrombosis and Hemostasis, 2012, 38. vsk, nro 1, s. 47–54. PubMed:22314603. doi:10.1055/s-0031-1300951. ISSN 0094-6176. Artikkelin verkkoversio. (englanniksi)
worldcat.org
K. Chapman, M. Seldon, R. Richards: Thrombotic microangiopathies, thrombotic thrombocytopenic purpura, and ADAMTS-13. Seminars in Thrombosis and Hemostasis, 2012, 38. vsk, nro 1, s. 47–54. PubMed:22314603. doi:10.1055/s-0031-1300951. ISSN 0094-6176. Artikkelin verkkoversio. (englanniksi)
P. D. James, D. Lillicrap: The molecular characterization of von Willebrand disease: good in parts. British journal of haematology, 2013, 161. vsk, nro 2, s. 166–176. PubMed:23406206. doi:10.1111/bjh.12249. ISSN 0007-1048. Artikkelin verkkoversio. (englanniksi)
J. M. Johnsen et al: Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project. Blood, 2013, 122. vsk, nro 4, s. 590–597. PubMed:23690449. doi:10.1182/blood-2013-02-485094. ISSN 0006-4971. Artikkelin verkkoversio. (englanniksi)