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[Prenatal Diagnosis of A Case of SEA-HPFH Deletion Combined with Beta-Thalassemia in A Chinese Family].

Zhongguo shi yan xue ye xue za zhi - 1 Aug 2017

Chen Mei-Huan, Huang Hai-Long, Wang Yan, Zhang Min, Lin Na, He De-Qin, Lin Yuan, Xu Liang-Pu

Abstract excerpt

OBJECTIVE: To investigate the prenatal diagnosis of a case of SEA-HPFH deletion combined with beta-thalassemia in a Chinese family. METHODS: Gap-PCR and RDB methods were applied to test the genotype for the family. RESULTS: Mother showed a SEA-HPFH thalasemia trait phenotype, while her genotype was heterozygote for SEA-HPFH deletion; father showed a beta-thalassemia trait phenotype, while his genotype was...

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Source

Identifiers

PMID: 28823283
DOI: 10.7534/j.issn.1009-2137.2017.04.032

Genes

SEA

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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