Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach
Waye, John S, Riemer, Cathy, Gallivan, Monica V E, Kollia, Panagoula, Galanello, Renzo, Perseu, Lucia, Anstee, David J, Faustino, Paula, Harteveld, Cornelis L, Hoyer, James D, Peterson, Kenneth R, Giordano, Piero C, Stojiljkovic, Maja, Schrijver, Iris, Thein, Swee Lay, Gibbons, Richard J, Jarvis, Martin, Hardison, Ross C, Maglott, Donna, Francina, Alain, Borg, Joseph, Wada, Takahito, Basak, A Nazli, Giardine, Belinda, Pavlovic, Sonja, Costa, Flavia C, Papadopoulos, Petros, Old, John, Philipsen, Sjaak, Menzel, Stephan, Higgs, Douglas R, Radmilovic, Milena, Wajcman, Henri, Patrinos, George P, Fedosyuk, Halyna, Georgitsi, Marianthi, Traeger-Synodinos, Jan, Papadakis, Manoussos N, Joly, Philippe, Papachatzopoulou, Adamantia, Tully, Ray, Miller, Webb, Zukic, Branka, Felice, Alex E, Kanavakis, Emmanuel, Singleton, Belinda K, Wiemann, Claudia, Moradkhani, Kamran, Satta, Stefania, Clark, Barnaby, Chui, David H K
Published in Nature genetics (01.04.2011)
Published in Nature genetics (01.04.2011)
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New and Known β-Thalassemia Determinants Masked by Known and New δ Gene Defects [Hb A2-Ramallah or δ6(A3)Glu→Gln, GAG>>CAG]
Phylipsen, Marion, Harteveld, Cornelis L., Metz, Menno de, Gallivan, Monica V.E., Arkesteijn, Sandra G.J., Luo, Hong-Yuan, Chui, David H.K., Giordano, Piero C.
Published in Hemoglobin (01.10.2010)
Published in Hemoglobin (01.10.2010)
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Systematic documentation and analysis of human genetic variation using the microattribution approach
Giardine, Belinda, Borg, Joseph, Higgs, Douglas R., Peterson, Kenneth R., Maglott, Donna, Basak, A. Nazli, Clark, Barnaby, Faustino, Paula, Felice, Alex E., Francina, Alain, Gallivan, Monica V. E., Georgitsi, Marianthi, Gibbons, Richard J., Giordano, Piero C., Harteveld, Cornelis L., Joly, Philippe, Kanavakis, Emmanuel, Kollia, Panagoula, Menzel, Stephan, Miller, Webb, Moradkhani, Kamran, Old, John, Papachatzopoulou, Adamantia, Papadakis, Manoussos N., Papadopoulos, Petros, Pavlovic, Sonja, Philipsen, Sjaak, Radmilovic, Milena, Riemer, Cathy, Schrijver, Iris, Stojiljkovic, Maja, Thein, Swee Lay, Traeger-Synodinos, Jan, Tully, Ray, Wada, Takahito, Waye, John, Wiemann, Claudia, Zukic, Branka, Chui, David H. K., Wajcman, Henri, Hardison, Ross C., Patrinos, George P.
Published in Nature genetics (20.03.2011)
Published in Nature genetics (20.03.2011)
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Secondary mutation (c.94_95delAG) in a -α3.7 allele associated with Hb H disease in two unrelated African American individuals homozygous for the -α(3.7) deletion (-α3.7/-α3.7T)
Zhao, Po, Buller-Burckle, Arlene M, Peng, Mei, Anderson, Alison, Han, Z Jenny, Gallivan, Monica V E
Published in Hemoglobin (2012)
Published in Hemoglobin (2012)
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Compound Heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (Aγ81Leu-β86Ala) in a Ugandan Woman
Han, Zeqiu J., Lapuz, Cristina, Rovenger, Jill F., Dreyfus, Peter A., Vispo, Beverly G., Ou, Ching-Nan, Luo, Hong-Yuan, Chui, David H.K., Gallivan, Monica V.E.
Published in Hemoglobin (01.06.2012)
Published in Hemoglobin (01.06.2012)
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