Non ‐invasive prenatal testing for fetal inheritance of maternal β‐thalassaemia mutations using targeted sequencing and relative mutation dosage: a feasibility study

ConclusionsRMD for detection of inheritance of maternal β‐thalassaemia mutations has potential for clinical use. Our sequential approach could be applied to other single‐gene disorders.This article is protected by copyright. All rights reserved.
Source: BJOG: An International Journal of Obstetrics and Gynaecology - Category: OBGYN Authors: Tags: Main Research Article Source Type: research
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