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Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.
Giardine B, Borg J, Higgs DR, Peterson KR, Philipsen S, Maglott D, Singleton BK, Anstee DJ, Basak AN, Clark B, Costa FC, Faustino P, Fedosyuk H, Felice AE, Francina A, Galanello R, Gallivan MV, Georgitsi M, Gibbons RJ, Giordano PC, Harteveld CL, Hoyer JD, Jarvis M, Joly P, Kanavakis E, Kollia P, Menzel S, Miller W, Moradkhani K, Old J, Papachatzopoulou A, Papadakis MN, Papadopoulos P, Pavlovic S, Perseu L, Radmilovic M, Riemer C, Satta S, Schrijver I, Stojiljkovic M, Thein SL, Traeger-Synodinos J, Tully R, Wada T, Waye JS, Wiemann C, Zukic B, Chui DH, Wajcman H, Hardison RC, Patrinos GP. Giardine B, et al. Among authors: francina a. Nat Genet. 2011 Mar 20;43(4):295-301. doi: 10.1038/ng.785. Nat Genet. 2011. PMID: 21423179 Free PMC article.
Phenotype determination of hemoglobinopathies by mass spectrometry.
Zanella-Cleon I, Joly P, Becchi M, Francina A. Zanella-Cleon I, et al. Among authors: francina a. Clin Biochem. 2009 Dec;42(18):1807-17. doi: 10.1016/j.clinbiochem.2009.04.010. Epub 2009 May 4. Clin Biochem. 2009. PMID: 19409377 Review.
Special issue: hemoglobin disorders.
Wajcman H, Francina A. Wajcman H, et al. Among authors: francina a. Clin Biochem. 2009 Dec;42(18):1743-4. doi: 10.1016/j.clinbiochem.2009.10.016. Clin Biochem. 2009. PMID: 19942028 No abstract available.
113 results