Prenatal Diagnosis of Hb Bart’s Hydrops Fetalis Caused by a Genetic Compound Heterozygosity for Two Different α<sup>o</sup>-Thalassemia Determinants-Reference-Cited by-同舟云学术

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Prenatal Diagnosis of Hb Bart’s Hydrops Fetalis Caused by a Genetic Compound Heterozygosity for Two Different α^o-Thalassemia Determinants

Published:2007 Issue:4 Volume:22 Page:264-268
ISSN:1015-3837
Container-title:Fetal Diagnosis and Therapy
language:en
Short-container-title:Fetal Diagn Ther

Author:

Siriratmanawong Nirut,Pinmuang-ngam Charnchai,Fucharoen Goonnapa,Fucharoen Supan

Publisher

S. Karger AG

Subject

Obstetrics and Gynaecology,Radiology Nuclear Medicine and imaging,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference23 articles.

1. Prevalence and Genotypes of α- and β-Thalassemia Carriers in Hong Kong — Implications for Population Screening

2. Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Characterisation of two unusual cases of haemoglobin Bart’s hydrops foetalis caused by –SEA and large novel α-globin gene cluster deletions;Journal of International Medical Research;2021-02

2. Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam;Hemoglobin;2019-09-03

3. An international registry of survivors with Hb Bart's hydrops fetalis syndrome;Blood;2017-03-09

4. Identification of a novel 44.6-kb deletion causing α0 -thalassemia in southern China;International Journal of Laboratory Hematology;2017-02-28

5. Occurrence of the – –SEA, – –THAIand – –FILα-Thalassemia-1 Carriers from a 7-Year Study at Ramathibodi Hospital, Bangkok, Thailand;Hemoglobin;2016-07-03

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