Prenatal diagnosis of 33 fetuses at risk of having Hb Bart’s hydrops fetalis syndrome caused by homozygous α<sup>0</sup>-thalassemia using the LAMP colorimetric assay for α<sup>0</sup>-thalassemia (SEA deletion) in comparison with a routine conventional gap-PCR.
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Prenatal diagnosis of 33 fetuses at risk of having Hb Bart’s hydrops fetalis syndrome caused by homozygous α0-thalassemia using the LAMP colorimetric assay for α0-thalassemia (SEA deletion) in comparison with a routine conventional gap-PCR.
创建时间：
2022-04-28
