The search for SNPs, CNVs, and epigenetic variants associated with the complex disease of male infertility
Author:
Publisher
Informa UK Limited
Subject
Urology,Reproductive Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/19396368.2010.521615
Reference120 articles.
1. Single nucleotide polymorphisms of the gonadotrophin-regulated testicular helicase (GRTH) gene may be associated with the human spermatogenesis impairment
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3. Mutation analysis of the X-chromosome linked, testis-specific TAF7L gene in spermatogenic failure
4. Congenital Bilateral Absence of the Vas Deferens
5. Sperm protamine 1/protamine 2 ratios are related to in vitro fertilization pregnancy rates and predictive of fertilization ability
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