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• W2155163595 abstract "Abstract Association between the histidine‐rich glycoprotein ( HRG ) C633T single nucleotide polymorphism ( SNP ) and recurrent miscarriage was investigated in a case–control study. The cases constituted 187 women with recurrent miscarriage that were compared with 395 controls who had delivered a child and had no history of miscarriage. Blood samples were collected from each woman, genomic DNA was extracted and genotyped for the HRG C633T SNP . In the whole study population, the percentage of miscarriage was the same, regardless of genotype (C/C 31.2%, C/T 32.9% and T/T 32.5%). However, an association between homozygous T/T carriers and recurrent miscarriage was detected in a subgroup of women with primary recurrent miscarriage (odds ratio 2.44, 95% CI 1.01–5.92). Our results indicate an important role for the HRG C633T SNP in the occurrence of recurrent miscarriage." @default.
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• W2155163595 date "2013-05-15" @default.
• W2155163595 modified "2023-10-06" @default.
• W2155163595 title "Histidine-rich glycoprotein gene polymorphism in patients with recurrent miscarriage" @default.
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• W2155163595 doi "https://doi.org/10.1111/aogs.12155" @default.
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