Diagnosing von Willebrand disease: genetic analysis

Goodeve, A. orcid.org/0000-0002-6177-7062 (2016) Diagnosing von Willebrand disease: genetic analysis. Hematology, The Education Program, 2016 (1). pp. 678-682. ISSN 1520-4391



Copyright, Publisher and Additional Information: © 2016 American Society of Hematology. This is an author produced version of a paper subsequently published in Hematology. Uploaded in accordance with the publisher's self-archiving policy.
Keywords: Base Sequence; Hemophilia A; High-Throughput Nucleotide Sequencing; Humans; Multiplex Polymerase Chain Reaction; Sequence Deletion; von Willebrand Disease, Type 2; von Willebrand Disease, Type 3
  • Published (online): 2 December 2016
  • Published: 2 December 2016
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > Department of Infection, Immunity and Cardiovascular Disease
The University of Sheffield > Sheffield Teaching Hospitals
Depositing User: Symplectic Sheffield
Date Deposited: 22 Jun 2017 13:13
Last Modified: 02 Dec 2017 01:38
Published Version: https://doi.org/10.1182/asheducation-2016.1.678
Status: Published
Publisher: American Society of Hematology
Refereed: Yes
Identification Number: https://doi.org/10.1182/asheducation-2016.1.678
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