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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: Nov 23, 2021. (Total: 3579 publications since 2011)
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Records 1-6 (of 6 Records)
Query Trace: all>>Connie H Miller[CDC Author]
Genetic causes of haemophilia in women and girls.
Connie H Miller, and Christopher J Bean
Haemophilia : the official journal of the World Federation of Hemophilia 2020 Dec
Evaluation of CDC's Hemophilia Surveillance Program - Universal Data Collection (1998-2011) and Community Counts (2011-2019), United States.
Laura A Schieve, Vanessa R Byams, Brandi Dupervil, Meredith A Oakley, Connie H Miller, J Michael Soucie, Karon Abe, Christopher J Bean, and W Craig Hooper
Morbidity and mortality weekly report. Surveillance summaries (Washington, D.C. : 2002) 2020 Sep 69(5) 1-18
Mutation analysis of a cohort of US patients with hemophilia B.
Tengguo Li, Connie H Miller, Jennifer Driggers, Amanda B Payne, Dorothy Ellingsen, and W Craig Hooper
Am. J. Hematol. 2014 Apr 89(4) 375-9
The CDC Hemophilia A Mutation Project (CHAMP) mutation list: a new online resource.
Amanda B Payne, Connie H Miller, Fiona M Kelly, J Michael Soucie, and W Craig Hooper
Hum. Mutat. 2013 Feb 34(2) E2382-91
The CDC Hemophilia B mutation project mutation list: a new online resource.
Tengguo Li, Connie H Miller, Amanda B Payne, and W Craig Hooper
Mol Genet Genomic Med 2013 Nov 1(4) 238-45
F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis.
Samantha C Gouw, H Marijke van den Berg, Johannes Oldenburg, Jan Astermark, Philip G de Groot, Maurizio Margaglione, Arthur R Thompson, Waander van Heerde, Jorien Boekhorst, Connie H Miller, Saskia le Cessie, and Johanna G van der Bom
Blood 2012 Mar 22. 119(12) 2922-34
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