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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1991 | 2 |
2021 | 1 |
2024 | 0 |
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GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis.
J Thromb Haemost. 2021 Oct;19(10):2612-2617. doi: 10.1111/jth.15459. Epub 2021 Aug 5.
J Thromb Haemost. 2021.
PMID: 34355501
Free PMC article.
Molecular basis of von Willebrand disease type IIB. Candidate mutations cluster in one disulfide loop between proposed platelet glycoprotein Ib binding sequences.
Randi AM, Rabinowitz I, Mancuso DJ, Mannucci PM, Sadler JE.
Randi AM, et al.
J Clin Invest. 1991 Apr;87(4):1220-6. doi: 10.1172/JCI115122.
J Clin Invest. 1991.
PMID: 2010538
Free PMC article.
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An Arg545----Cys545 substitution mutation of the von Willebrand factor in type IIB von Willebrand's disease.
Donnér M, Andersson AM, Kristoffersson AC, Nilsson IM, Dahlbäck B, Holmberg L.
Donnér M, et al.
Eur J Haematol. 1991 Nov;47(5):342-5. doi: 10.1111/j.1600-0609.1991.tb01858.x.
Eur J Haematol. 1991.
PMID: 1761120
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