A large deletion identified in a Swedish family with type 1 VWD
| Autor: | Elsa Lanke, Stefan Lethagen, Torbjörn Säll, Anna Johansson, Christer Halldén |
|---|---|
| Rok vydání: | 2011 |
| Předmět: |
Pathology
medicine.medical_specialty MEDLINE Hemorrhage Penetrance Bioinformatics Polymorphism Single Nucleotide von Willebrand Disease Type 1 Text mining Type (biology) Polymorphism (computer science) von Willebrand Factor medicine Von Willebrand disease Humans Family Sequence Deletion Sweden business.industry Haplotype Hematology medicine.disease Thrombosis Pedigree Haplotypes business Microsatellite Repeats |
| Zdroj: | Thrombosis and Haemostasis. 105:733-734 |
| ISSN: | 2567-689X 0340-6245 |
| DOI: | 10.1160/th10-08-0556 |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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