A Double Heterozygote for (δβ)⁰-Thalassemia and Codons 41/42 (–TTCT) Behaves as a Homozygote for the Frameshift Mutation in a Chinese Family

Can Liao Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China

Qiong Feng Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China

Jian Li Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China

Yining Huang Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of China

Dongzhi Li Prenatal Diagnostic Center, Guangzhou Maternal & Neonatal Hospital, Guangzhou Medical College, Guangzhou, Guangdong, People's Republic of ChinaCorrespondence[email protected]

REFERENCES

Li D, Liao C, Li J, Huang Y, Xie X, Wei J, Wu S. Prenatal diagnosis of β-thalassemia by reverse dot-blot hybridization in Southern China. Hemoglobin 2006; 30(3)365–370
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Peng CT, Liu SC, Chiou SS, Kuo PL, Shih MC, Chang JY, Chang JG. Molecular characterization of deletional forms of β-thalassemia in Taiwan. Ann Hematol 2003; 82(1)33–36
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A Double Heterozygote for (δβ)⁰-Thalassemia and Codons 41/42 (–TTCT) Behaves as a Homozygote for the Frameshift Mutation in a Chinese Family

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A Double Heterozygote for (δβ)0-Thalassemia and Codons 41/42 (–TTCT) Behaves as a Homozygote for the Frameshift Mutation in a Chinese Family

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A Double Heterozygote for (δβ)⁰-Thalassemia and Codons 41/42 (–TTCT) Behaves as a Homozygote for the Frameshift Mutation in a Chinese Family