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Additional file 1 of Estimating the frequency of causal genetic variants in foetuses with congenital heart defects: a Chinese cohort study

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posted on 2022-01-05, 04:45 authored by Fengying Lu, Peng Xue, Bin Zhang, Jing Wang, Bin Yu, Jianbin Liu
Additional file 1. Supplementary table 1. The specific primer sequences of Sanger sequencing.

Funding

changzhou key laboratory of high-tech research changzhou social development science and technology support project jiangsu maternal and children healthcare key discipline science and technology development fund of nanjing medical university

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    Orphanet Journal of Rare Diseases

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    Keywords

    Congenital heart defectsChromosomal abnormalitiesCopy number variationsChromosome microarray analysisWhole exome sequencing

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