REFERENCES
- Masala B, Manca L. Detection of the common Hb F Sardinia [Aγ75(E19)Ile→Thr] variant by isoelectric focusing in normal newborn and adult affected by elevated fetal hemoglobin syndromes. Clin Chim Acta. 1991;198(3):195–202.
- Manca L, Formato M, Demuro P, . The γ globin chain heterogeneity of the Sardinian newborn baby. Hemoglobin. 1986;10(5):519–528.
- Masala B, Manca L. Separation of globin chains by reversed-phase high-performance liquid chromatography. Methods Enzymol. 1994;231:21–44.
- Manca L, Masala B. Disorders of the synthesis of human fetal hemoglobin. IUMB Life. 2008;60(2):94–111.
- Shen SH, Slightom JL, Smithies O. A history of the human fetal globin gene duplication. Cell. 1981;26(2):191–203.
- Moo-Penn WF, Bechtel KC, Johnson MH, . Hemoglobin Fannin-Lubock [α2β2119 (GH2)Gly→Asp]. A new hemoglobin variant at the α1β1 contact. Biochim Biophys Acta. 1976; 453(2):472–477.
- Chen-Marotel J, Braconnier F, Blouquit Y, Martin-Caburi J, Kammerer J, Rosa J. Hemoglobin Bougardirey-Mali β119 (GH2) Gly→Val. An electrophoretically silent variant migrating in isoelectrofocusing as Hb F. Hemoglobin. 1979;3(4):253–262.
- Plaseska D, de Alarcon PA, McMillan S, Walbrecht M, Wilson JB, Huisman THJ. Hb Iowa or α2β2119(GH2)Gly→Ala. Hemoglobin. 1990;14(4):423–429.
- Duarte DF, Albuquerque DM, Pereira Pinheiro VR, Ferreira Costa F, Da Fátima Sonati M. Three new structural variants of fetal hemoglobin: Hb F-Campinas [Aγ121(GH4)Glu→Gln], Hb F-Paulinia [Gγ80(EF4)Asp→Tyr] and Hb F-Joanopolis [Gγ73(E17)Asp→Ala]. Haematologica. 2003;88(11):1316–1317.
- Nakatsuji T, Lam H, Carver J, Huisman THJ. Hb F-Marietta or GγI80(EF4)Asp→Asn, observed in a Caucasian baby. Hemoglobin. 1982;6(4):407–411.
- Huisman THJ. Gamma chain abnormal human fetal hemoglobin variants. 1997;55(3):159–163.
- Sack JS, Andrews LC, Magnus, KA, Hanson JC, Rubin J, Love WE. Location of amino acid residues in human deoxy hemoglobin. Hemoglobin. 1978;2(2):153–169.
- Blackwell RQ, Yang HJ, Wang CC. Hemoglobin G-Szuhu: β80 Asn→Lys. Biochim Biophys Acta. 1969;188(1):59–64.
- Préhu C, Riou J, Henthorn J, Wajcman H. A new silent β chain variant: Hb Hounslow [β80(EF4)Asn→Tyr]. Balkan J Med Genet. 2007;10(1):29–32.