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scopus: 34568906600

Chui, D.H.

(David Chui)


mutation variant globin database genome hemoglobin information ucsc genome browser hbvar browser sequence hb variants phenotype hemoglobin variants region table thalassemia report hba 2 genes example query result university thalassemia mutations α- globin gene α- globin genes reference b-thalassemia chain conversion hba 1 locus winnipeg genome browser track locus variants track population encode gene conversion events genomic percentage study b-thalassemia mutations project event analysis deletion cause hekinan hba 2 number hbvar database medicine patrino phencode disease α2/α1 ratio frequency issue sample research family blood hardison pennsylvania state university acids research chromosome protein color ¢ gure encode project consortium tables 2 hba 1 genes gene conversion miller background hb variant gerland entry stanleyville-ii α2/α1




3 Most Recent Publications

Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants (Article)
Moradkhani, K. Prehu, C. Old, J. Henderson, S. Balamitsa, V. Luo, H-Y. Poon, M-C. Chui, D.H. Wajcman, H. Patrinos, G.P.
2008-01-01
PhenCode: Connecting ENCODE data with mutations and phenotype (Article)
Giardine, B. Riemer, C. Kern, A. Kuhn, R. Patrinos, G.P. Hughes, J. Higgs, D. Chui, D.H. Scriver, C.R. Phommarinh, M. Patnaik, S.K. Blumenfeld, O. Hefferon, T. Gottlieb, B. Vihinen, M. Väliaho, J. Kent, J. Miller, W. Hardison, R. Thomas, D. Hsu, F. Zielenski, J. Sang, Y. Elnitski, L. Cutting, G. Trumbower, H.
2007-06-01
Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies. (Article)
Patrinos, G.P. Giardine, B. Riemer, C. Miller, W. Chui, D.H. Anagnou, N.P. Wajcman, H. Hardison, R.C.
2004-01-01