Johansson, Anna M <br/><br/>
A large deletion identified in a Swedish family with type 1 VWD.  [electronic resource] 

 -  Thrombosis and haemostasis  Apr 2011 
 - 733-4 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2567-689X 
<br/><br/><label>Standard No.: </label>10.1160/TH10-08-0556  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Family<br/>Haplotypes<br/>Hemorrhage<br/>Humans<br/>Microsatellite Repeats--genetics<br/>Pedigree<br/>Penetrance<br/>Polymorphism, Single Nucleotide<br/>Sequence Deletion--genetics<br/>Sweden<br/>von Willebrand Disease, Type 1--blood<br/>von Willebrand Factor--genetics