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Article

Molecular characterization of a Chinese pedigree with beta-thalassemia intermedia.

Hemoglobin - 1 Jan 2010

Huang Ge, Jiang Wen-Ling, Rong Ka-Bin, Li Yun-Xiong, Luo Xian-Ling, Meng Jin-Xiu, Yu Xi-Yong

Abstract excerpt

Hereditary persistence of fetal hemoglobin (HPFH), often associated with mutations in the beta-globin gene cluster, is normally benign, but a person carrying both HPFH and another beta-thalassemia (beta-thal) mutation will develop serious anemia. These people might be erroneously diagnosed as having homozygous beta-thal with common reverse dot-blot methods. Here we report a 5-year old boy with thalassemia...

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Identifiers

PMID: 20353356
DOI: 10.3109/03630261003670226

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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