Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome

A genetic origin is estimated in 30% of infertile men with the common phenotypes of oligo- or azoospermia, but the pathogenesis of spermatogenic failure remains frequently obscure. To determine the involvement of Copy Number Variants (CNVs) in the origin of male infertility, patients with idiopathic...

Descripción completa

Detalles Bibliográficos
Autores principales: Tüttelmann, Frank, Simoni, Manuela, Kliesch, Sabine, Ledig, Susanne, Dworniczak, Bernd, Wieacker, Peter, Röpke, Albrecht
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084853/
https://www.ncbi.nlm.nih.gov/pubmed/21559371
http://dx.doi.org/10.1371/journal.pone.0019426

Ejemplares similares

Ejemplares similares