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Association of GDF1 rs4808863 with fetal congenital heart defects: a case–control study

14

Citations

21

References

2015

Year

Abstract

Our results suggest that the GDF1 rs4808863 polymorphism contributes to an increased risk of fetal CHDs, especially the subtypes of AVSD, LVOTO and left-right laterality defects.

References

YearCitations

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