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03 May 2021: Meta-Analysis

The Roles of Reduced Folate Carrier-1 (RFC1) A80G (rs1051266) Polymorphism in Congenital Heart Disease: A Meta-Analysis

Kang Yi 12ABCDEF* , Yu-Hu Ma 23ABCDEF* , Wei Wang 23BCF , Xin Zhang 24BCF , Jie Gao 23BCD , Shao-E He 25BCD , Xiao-Min Xu 23CDF , Meng Ji 23CDF , Wen-Fen Guo 6ADEG* , Tao You 12ABCDEFG*

DOI: 10.12659/MSM.929911

Med Sci Monit 2021; 27:e929911

Supplementary Table 1 The full detailed search strategy and searching terms.

SetQuery
#1TS=(“Heart Defects, Congenital” OR “congenital heart abnormalities” OR “congenital heart abnormality” OR “congenital heart malformation” OR “congenital heart defect” OR “congenital heart disease” OR “congenital heart defects” OR “congenital heart diseases”)
#2TS=(“atrial septal defects” OR “atrial septal defect”)
#3TS=(“ventricular septal defect” OR “ventricular septal defects”)
#4TS=(“Trilogy of Fallot” OR “Tetralogy of Fallot”)
#5TS=(“patent ductus arteriosus” OR “scimitar syndrome” OR “anomalous pulmonary venous connection”)
#6TS=(foramen oval OR lutembacher syndrome)
#7TS=(single ventricle OR univentricular heart)
#8TS=(“double inlet left ventricle” OR “double outlet right ventricle”)
#9TS=(“persistent truncus arteriosus” OR “persistent ostium primum” OR “interrupted aortic arch”)
#10TS=(“pulmonary valve stenoses” OR “pulmonary valve stenosis” OR “pulmonary stenoses” OR “pulmonary stenosis” OR “pulmonary valve stenosis” OR “pulmonic stenosis” OR “pulmonic stenoses”)
#11TS=(tricuspid atresia OR valve atresia)
#12TS=(“pulmonary atresia” OR “absent right atrioventricular connection”)
#13#1 OR #2 OR #3 OR #4 OR #5 OR #6 OR #7 OR #8 OR #9 OR #10 OR #11 OR #12
#14TS=(“solute carrier family 19 member 1” OR “Reduced folate carrier” OR “folate transporter 1” OR “intestinal folate carrier 1” OR “placental folate transporter” OR “reduced folate carrier protein” OR SLC19A1 OR RFC OR RFC-1 OR IFC1 OR IFC-1)
#15TS=(“Polymorphism, Single Nucleotide” OR Genotype OR Alleles OR polymorphism OR “genetic variant” OR “genetic variants” OR “genetic polymorphism” OR genetic OR “Genetic Variation” OR SNP OR mutation OR variation OR variant OR “single nucleotide polymorphism”)
#16#13 AND #14 AND #15

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Medical Science Monitor Basic Research eISSN: 2325-4416
Medical Science Monitor Basic Research eISSN: 2325-4416