β-Thalassemia Mutation At Codon 37 (Tgg>>Tga) Detected In A Turkish Family
暂无分享,去创建一个
[1] M. H. Muslumanoglu,et al. Nonsense β-Thalassemia Mutation at Codon 37 (TGG>TGA), Detected for the First Time in Three Turkish Cases , 2012, Hemoglobin.
[2] Xue-wei Tang,et al. The Codon 37 (TGG→TAG) β0-Thalassemia Mutation Found in a Chinese Family , 2006, Hemoglobin.
[3] H. Birgens,et al. β-Thalassemia Due to a Novel Nonsense Mutation at Codon 37 (TGG→TAG) Found in an Afghanistani Family , 2005, Hemoglobin.
[4] Alla Joutovsky,et al. HPLC retention time as a diagnostic tool for hemoglobin variants and hemoglobinopathies: a study of 60000 samples in a clinical diagnostic laboratory. , 2004, Clinical chemistry.
[5] T. Huisman,et al. Molecular characterization of beta-thalassemia in north Jordan. , 1994, Hemoglobin.
[6] M. Baiget,et al. HIGH PREVALENCE OF THE β‐THALASSAEMIA NONSENSE 37 MUTATION IN CATALONIANS FROM THE EBRO DELTA , 1992, British journal of haematology.
[7] P. Waber,et al. Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian family [published erratum appears in Blood 1986 Jul;68(1):323] , 1986 .
[8] E. Abraham,et al. On the chromatographic heterogeneity of human fetal hemoglobin. , 1979, Biochimica et biophysica acta.
[9] H. Kazazian,et al. Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian family. , 1986, Blood.