-transparent.png){kind=logo}
We report the characterization of the amount of beta mRNA in a Kurdish Jewish population with beta0-thalassemia using the same methods employed for characterization of the Catania and Ferrara beta0 patients. We found very low amounts of beta mRNA sequences, consistent with the presence of beta0-thalassemia of the beta mRNA-negative population type. In addition, no globin gene deletion was detected that could account for the absence of beta mRNA.
Related Publications
F Ramirez, and
D Starkman, and
A Bank, and
H Kerem, and
G Cividalli, and
E A Rachmilewitz
November 1978,
Israel journal of medical sciences,
F Ramirez, and
D Starkman, and
A Bank, and
H Kerem, and
G Cividalli, and
E A Rachmilewitz
January 1977,
Hemoglobin,
F Ramirez, and
D Starkman, and
A Bank, and
H Kerem, and
G Cividalli, and
E A Rachmilewitz
January 1973,
Israel journal of medical sciences,
F Ramirez, and
D Starkman, and
A Bank, and
H Kerem, and
G Cividalli, and
E A Rachmilewitz
January 1988,
Hemoglobin,
F Ramirez, and
D Starkman, and
A Bank, and
H Kerem, and
G Cividalli, and
E A Rachmilewitz
June 1978,
Cell,
F Ramirez, and
D Starkman, and
A Bank, and
H Kerem, and
G Cividalli, and
E A Rachmilewitz
January 1978,
Hemoglobin,
F Ramirez, and
D Starkman, and
A Bank, and
H Kerem, and
G Cividalli, and
E A Rachmilewitz
November 1959,
Harefuah,
F Ramirez, and
D Starkman, and
A Bank, and
H Kerem, and
G Cividalli, and
E A Rachmilewitz
June 1978,
Cell,
F Ramirez, and
D Starkman, and
A Bank, and
H Kerem, and
G Cividalli, and
E A Rachmilewitz
September 1966,
British journal of haematology,
F Ramirez, and
D Starkman, and
A Bank, and
H Kerem, and
G Cividalli, and
E A Rachmilewitz
December 1981,
Cell,
