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CDC-Authored Genomics and Precision Health Publications Database|Home|PHGKB

CDC-Authored Genomics and Precision Health Publications Database


Last data update: Jun 09, 2021. (Total: 3321 publications since 2011)
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Records 1-3 (of 3 Records)
Query Trace: all>>C H Miller[CDC Author]
Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations.
B Boylan, A S Rice, C De Staercke, M E Eyster, H M Yaish, C M Knoll, C J Bean, C H Miller, and
J. Thromb. Haemost. 2015 Jun 13(6) 1036-42
Utility of multiplex ligation-dependent probe amplification (MLPA) for hemophilia mutation screening.
A B Payne, C J Bean, W C Hooper, and C H Miller
J. Thromb. Haemost. 2012 Sep 10(9) 1951-4
F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity.
C H Miller, J Benson, D Ellingsen, J Driggers, A Payne, F M Kelly, J M Soucie, W Craig Hooper, and
Haemophilia 2012 May 18(3) 375-82
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