Table S2 BGI Genomics CHD Prenatal Diagnose (IMAGE)

BGI Genomics

Table S2 BGI Genomics CHD Prenatal Diagnose

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Table S2. Secondary findings identified in the study. AD, autosomal dominant; AR, autosomal recessive. Het, heterozygous; TOF, tetralogy of Fallot; TGA, d-transposition of great arteries; RVOTD, right ventricular outflow tract defect; CHD, congenital heart defect; LP, likely pathogenic;

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