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A large deletion identified in a Swedish family with type 1 VWD.
Anna M Johansson, Elsa Lanke, Torbjörn Säll, Stefan Lethagen, Christer Halldén
Thrombosis and haemostasis 2011 Apr
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Citation
Anna M Johansson, Elsa Lanke, Torbjörn Säll, Stefan Lethagen, Christer Halldén.
A large deletion identified in a Swedish family with type 1 VWD.
Thrombosis and haemostasis.
2011 Apr;105(4):733-4
Mesh Tags
Family
Haplotypes
Hemorrhage
Humans
Microsatellite Repeats
Pedigree
Penetrance
Polymorphism, Single Nucleotide
Sequence Deletion
Sweden
von Willebrand Disease, Type 1
von Willebrand Factor
Substances
von Willebrand Factor
PMID: 21225094
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