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- W2478212852 abstract "Abstract Infertility is a common cause for gynaecological consultation, with male factor infertility the most common cause. This case illustrates the importance of thorough history taking and examination in any couple presenting with infertility. In this case a clinical diagnosis of congenital unilateral absence of the vas deferens prompted genetic testing of both partners, and identified the risk of a pregnancy affected by cystic fibrosis. Intracytoplasmic sperm injection (ICSI) followed by prenatal genetic diagnosis (PGD) of the resulting embryo allowed the couple, both carriers of a mutation of the Cystic Fibrosis Transmembrane Regulator (CFTR) gene, to achieve a successful healthy pregnancy." @default.
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- W2478212852 date "2015-01-01" @default.
- W2478212852 modified "2023-10-17" @default.
- W2478212852 title "Pre-implantation genetic diagnosis in oligozoospermia" @default.
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- W2478212852 doi "https://doi.org/10.1093/med/9780199654994.003.0004" @default.
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