Article

Analysis of genomic copy number variation in 48 azoospermia patients with chromosomal abnormalities

2023-03-16

Abstract excerpt

<h4>Background: </h4> To explore the copy number variation (CNV) of genome in azoospermia patients with chromosomal abnormalities, and to lay a foundation for elucidating the genetic factors of spermatogenesis. <h4>Methods: </h4> 204 patients with azoospermia were analyzed by G banding karyotype analysis; The next generation sequencing technology (NGS) is used to detect CNV, screen out CNVs related genes, and det...

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Literature Corpus work: c1c0934d-d088-5f58-93b2-57c949dac97a
DOI: 10.21203/rs.3.rs-2678174/v1

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