What is the role of genetic testing in the investigation of patients with suspected platelet function disorders?-Reference-Cited by-同舟云学术

What is the role of genetic testing in the investigation of patients with suspected platelet function disorders?

Published:2014-01-30 Issue:2 Volume:165 Page:193-203
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Daly Martina E.¹,Leo Vincenzo C.¹,Lowe Gillian C.²,Watson Steve P.²,Morgan Neil V.²

Affiliation:

1. Department of Cardiovascular Science; University of Sheffield Medical School; University of Sheffield; Sheffield UK

2. Centre for Cardiovascular Sciences; School of Clinical and Experimental Medicine; College of Medical and Dental Sciences; University of Birmingham; Birmingham UK

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.12751/fullpdf

Reference60 articles.

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2. Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome;Albers;Nature Genetics,2012

3. Genetics of familial forms of thrombocytopenia;Balduini;Human Genetics,2012

4. Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias;Balduini;British Journal of Haematology,2011

5. Inherited thrombocytopenias frequently diagnosed in adults;Balduini;Journal of Thrombosis and Haemostasis,2013

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