Rapid detection of point mutations and polymorphisms of the α-globin genes by DGGE and SSCA
Harteveld KL, Heister AJ, Giordano PC, Losekoot M, Bernini LF. Rapid detection of point mutations and polymorphisms of the α-globin genes by DGGE and SSCA. Hum Mutat 1996;7:114-22.
The -158 (C→T) promoter mutation is responsible for the increased transcription of the 3′ gamma gene in the Atlanta type of hereditary persistence of fetal hemoglobin
Efremov DG, Dimovski AJ, Huisman TH. The -158 (C→T) promoter mutation is responsible for the increased transcription of the 3′ gamma gene in the Atlanta type of hereditary persistence of fetal hemoglobin. Blood 1994;83: 3350-5.
HbVar: A relational base of human hemoglobin variants and thalassemia mutations at the globin gene server
Hardison RC, Chui DH, Giardine B, Riemer C, Patrinos GP, Anagnou N, et al. HbVar: a relational base of human hemoglobin variants and thalassemia mutations at the globin gene server. Hum Mutat 2002;19:225-33.
Hemoglobin variant HbG-Coushatta (β-22 Glu→Ala) found by dissociation of blood glucose from values of HbA1C measured by HPLC
Ogawa K, Bando T, Ogawa M, Miyazaki A, Nakanishi T, Shimizu A. Hemoglobin variant HbG-Coushatta (β-22 Glu→Ala) found by dissociation of blood glucose from values of HbA1C measured by HPLC. Intern Med 2003;42:781-7.
Variation of HbF and F-cell number with the G-γ Xmn I (C-T) polymorphism in normal individuals
Sampietro M, Thein SL, Contreras M, Pazmany L. Variation of HbF and F-cell number with the G-γ Xmn I (C-T) polymorphism in normal individuals. Blood 1992;79:832-3.
