References
- Schroeder W A, Huisman T HJ, Shelton J R, Shelton J B, Kleihauer E F, Dozy A M, Robberson B. Evidence for multiple structural genes for the γ chain of human fetal hemoglobin. Proc Natl Acad Sci USA 1968; 60(2)537–544
- Hardison R C, Chui D HK, Riemer C, Giardine B, Lehvaslaiho H, Wajcman H, Miller W. Databases of Human Hemoglobin Variants and Other Resources at the Globin Gene Server, http://globin.cse.psu.edu/hbvar/menu.html
- Grifoni V, Kamuzora H, Lehmann H, Charlesworth D. A new Hb variant: Hb F Sardinia γ75(E19) isoleucine leads to threonine found in a family with Hb G‐Philadelphia, β‐chain deficiency and a Lepore‐like haemoglobin indistinguishable from Hb A2. Acta Haematol 1975; 53(6)347–355
- Huisman T HJ, Kutlar F, Gu L‐H. γ Chain abnormalities and γ‐globin gene rearrangements in newborn babies of various populations. Hemoglobin 1991; 15(5)349–379
- Shelton J B, Shelton J R, Schroeder W A. High performance liquid chromatographic separation of globin chains on a large‐pore C4 column. J Liq Chromatogr 1984; 7(10)1969–1977
- Alter B P, Goff S C, Efremov G D, Gravely M E, Huisman T HJ. Globin chain electrophoresis: a new approach to the determination of the Gγ/Aγ ratio in fetal haemoglobin and to studies of globin synthesis. Br J Haematol 1980; 44(4)527–534
- Masala B, Manca L. Detection of the common Hb F Sardinia [Aγ75(E19)Ile→Thr] variant by isoelectric focusing in normal newborn and in adults affected by elevated fetal hemoglobin syndromes. Clin Chim Acta 1991; 198(3)195–202
- Manca L, Formato M, Demuro P, Pilo G, Gallisai D, Orzalesi M, Masala B. The γ globin chain heterogeneity of the Sardinian newborn baby. Hemoglobin 1986; 10(5)519–528
- Masala B, Manca L. Detection of globin chains by reversed‐phase high‐performance liquid chromatography. Methods Enzymol 1994; 231(1)21–44
- Huisman T HJ. Separation of hemoglobins and hemoglobin chains by high‐performance liquid chromatography. J Chromatogr 1987; 418(17)277–304
- Manca L, Cocco E, Gallisai D, Masala B, Gilman J G. Diminished AγT fetal globin levels in Sardinia haplotype II β0‐thalassemia patients are associated with the four base pair deletion in the AγT promoter. Br J Haematol 1991; 78(1)105–107
- Plaseska D, Kutlar F, Wilson J B, Fei Y J, Huisman T HJ. Hb F‐Charlotte, an Aγ variant with a threonine residue in position γ75 and a glycine residue in position γ136. Hemoglobin 1990; 14(6)617–625
- Huisman T HJ. Gamma chain abnormal human fetal hemoglobin variants. Am J Hematol 1997; 55(3)159–163
- Fuyuno K, Torigoe T, Ohba Y, Matsuoka M, Miyaji T. Survey of cord blood hemoglobin in Japan and identification of two new γ chain variants. Hemoglobin 1981; 5(2)139–151
- Nakatsuji T, Ohba Y, Huisman T HJ. Hb F‐Yamaguchi [γ75Thr, γ80Asn, γ136Ala) is associated with Gγ‐thalassemia. Am J Hematol 1984; 16(2)189–192
- Brimhall B, Vedvick T S, Jones R T, Ahern E, Palomino E, Ahern V. Haemoglobin F Port Royal (α2Gγ2 125Glu→Ala). Br J Haematol 1974; 27(2)313–318