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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.

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Figshare2022-04-28 更新2026-04-28 收录
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https://figshare.com/articles/dataset/Prenatal_diagnosis_of_33_fetuses_at_risk_of_having_Hb_Bart_s_hydrops_fetalis_syndrome_caused_by_homozygous_sup_0_sup_-thalassemia_using_the_LAMP_colorimetric_assay_for_sup_0_sup_-thalassemia_SEA_deletion_in_comparison_with_a_routine_convent/19677372
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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.
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2022-04-28
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