CDC-Authored Genomics and Precision Health Publications Database
Last data update: May 22, 2023. (Total: 4299 publications since 2011)
Query Trace: all>>Connie H Miller[CDC Author] |
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Genetic causes of haemophilia in women and girls.
Miller CH , Bean CJ . Haemophilia 2020 27 (2) e164-e179 |
Evaluation of CDC's Hemophilia Surveillance Program - Universal Data Collection (1998-2011) and Community Counts (2011-2019), United States.
Schieve LA , Byams VR , Dupervil B , Oakley MA , Miller CH , Soucie JM , Abe K , Bean CJ , Hooper WC . MMWR Surveill Summ 2020 69 (5) 1-18 |
The CDC Hemophilia B mutation project mutation list: a new online resource.
Li Tengguo, Miller Connie H, Payne Amanda B, Craig Hooper W. Mol Genet Genomic Med 2013 Nov 1(4) 238-45 . Mol Genet Genomic Med 2013 Nov 1(4) 238-45 |
Mutation analysis of a cohort of US patients with hemophilia B.
Li Tengguo, Miller Connie H, Driggers Jennifer, Payne Amanda B, Ellingsen Dorothy, Hooper W Craig. Am. J. Hematol. 2014 Apr 89(4) 375-9 . Am. J. Hematol. 2014 Apr 89(4) 375-9 |
The CDC Hemophilia A Mutation Project (CHAMP) mutation list: a new online resource.
Payne Amanda B, Miller Connie H, Kelly Fiona M, Michael Soucie J, Craig Hooper W. Hum. Mutat. 2013 Feb 34(2) E2382-91 . Hum. Mutat. 2013 Feb 34(2) E2382-91 |
F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis.
Gouw Samantha C, van den Berg H Marijke, Oldenburg Johannes, Astermark Jan, de Groot Philip G, Margaglione Maurizio, Thompson Arthur R, van Heerde Waander, Boekhorst Jorien, Miller Connie H, le Cessie Saskia, van der Bom Johanna G. Blood 2012 Mar 22. 119(12) 2922-34 . Blood 2012 Mar 22. 119(12) 2922-34 |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 22, 2023
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