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Miller, W.
(Webb Miller)
mutation database information hbvar b-thalassemia sequence ucsc genome browser b-thalassemia mutations hemoglobin variants query hemoglobin thalassemia population thalassemia mutations frequency variant genome acids research genomic region browser nucleotide alignment example research university miller output globin hardison bin size deletion spectrum globin gene server cell anemia foundation cause b-thalassemia ® eld nucleotide substitutions issue reference resource genomic dna sequences background populations /ethnic backgrounds hbvar database schwartz entry analysis promoter number country substitution server riemer hbvar users greek syllabu annotation /ethnic department mutation spectrum mutation frequencies figure cypriot frequency range speci ®c ccaat box science identi ®cation speci expression query page range study mediterranean cause reference sequence greek cypriots dna sequence pennsylvania state university
1 Most Recent Publications
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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
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