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- W2768461521 abstract "Genetic abnormalities are a common cause for male factor infertility and spermatogenic dysfunction. A key family of genetic disorders that arise from spontaneous mutations in the Y chromosome and are a common cause of male factor infertility are known as Y chromosome microdeletions (YCM). These deletions are associated with a range of clinical outcomes including severe oligospermia and azoospermia. In this article, we will discuss the history, etiology, diagnosis, and prevalence of YCM. We will also review the most common types and variations of YCM with current clinical management strategies, clinical data, and directions for future potential treatments." @default.
- W2768461521 created "2017-12-04" @default.
- W2768461521 creator A5011724751 @default.
- W2768461521 creator A5025350347 @default.
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- W2768461521 date "2018-01-01" @default.
- W2768461521 modified "2023-09-24" @default.
- W2768461521 title "Y Chromosome Microdeletions" @default.
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- W2768461521 doi "https://doi.org/10.1016/b978-0-12-801238-3.64538-5" @default.
- W2768461521 hasPublicationYear "2018" @default.
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