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Article

Electrophoresis features and genotypes of Hb bart's hydrops fetalis.

Scandinavian journal of clinical and laboratory investigation - 1 Jan 2000

Li Youqiong, Liang Liang, Tian Mao, Qing Ting, Wu Xin

Abstract excerpt

Hydrops fetalis syndrome (Hb Bart's disease) is one of the common fetal development abnormalities and the most severe form of α-thalassemia. It causes fetal death during the third trimester or shortly after birth. The aim of this study is to investigate the feature of Hb Bart's disease by Capillary electrophoresis (CE) and its genotypes. A total of 38 cases of suspected fetal Hb Bart's disease were analyzed by...

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Share to alpha-Thalassemia
Share to Electrophoresis, Capillary
Share to Fetal Blood

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Hemoglobins, Abnormal

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Share to Prenatal Diagnosis

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 31841045
DOI: 10.1080/00365513.2019.1703211

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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