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Bowen, D.J., Bowley, S., John, M. and Collins, P.W. (1998) Factor V Leiden (G1691A), the Prothrombin 3’-Untranslated Region Variant (G20210A) and Thermolabile Methylenetetrahydrofolate Reductase (C677T): A Single Genetic Test Genotypes All Three Loci—Determination of Frequencies in the S. Wales Population of the UK. Thrombosis and Haemostasis, 79, 949-954.
https://doi.org/10.1055/s-0037-1615100

has been cited by the following article:

• TITLE: Methylene Tetra-Hydrofolate Reductase Gene Polymorphism and Endometrial Perfusion in Unexplained Female Infertility

  AUTHORS: Eman Aly Abd El Fattah

  KEYWORDS: Unexplained Infertility, Uterine Doppler, MTHFR Gene Polymorphism

  JOURNAL NAME: Open Journal of Obstetrics and Gynecology, Vol.12 No.5, May 24, 2022

  ABSTRACT: Aim of the study: Examing the role of Methylene tetra-hydrofolate reductase (MTHFR C677T) polymorphisms in unexplained female infertility. Methods: The study was conducted on women with unexplained infertility attending the Infertility Clinic at El-Shatby University Hospital, Alexandria, during the period from October 2020 to October 2021. Uterine artery Doppler assessment and detection of MTHFR C677T gene mutation were done. The frequencies of homozygous and heterozygous gene mutations were determined. Results: In group I, 35 cases had abnormal uterine artery Doppler compared to 22 normal cases in group II. As regards MTHFR C677T gene mutation, 19 cases were positive in group I (7 were homozygous and 12 were heterozygous) and only one case was positive in group II (heterozygous) which was statistically significant. Conclusion: MTHFR C677T gene polymorphisms may play a role in unexplained infertility.