Molecular characterization of severe α-Thalassemias causing hydrops fetalis in Taiwan
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.1320390314/fullpdf
Reference23 articles.
1. Hydrops fetalis due to an unusual form of Hb H disease
2. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
3. Characterization of two deletions that remove the entire human ζ-α globin gene complex (—THAIand —FIL)
4. Molecular basis of length polymorphism in the human zeta-globin gene complex.
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2. Comparisons of serum non-transferrin-bound iron levels and fetal cardiac function between fetuses affected with hemoglobin Bart’s disease and normal fetuses;Frontiers in Medicine;2023-01-03
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