Microdeletions and microduplications linked to severe congenital disorders in infertile men

Data on the clinical validity of DNA copy number variants (CNVs) in spermatogenic failure (SPGF) is limited. This study analyzed the genome-wide CNV profile in 215 men with idiopathic SPGF and 62 normozoospermic fertile men, recruited at the Andrology Clinic, Tartu University Hospital, Estonia. A tw...

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Detalles Bibliográficos
Autores principales: Kikas, Triin, Punab, Anna Maria, Kasak, Laura, Poolamets, Olev, Vihljajev, Vladimir, Pomm, Kristjan, Reiman, Mario, Tjagur, Stanislav, Korrovits, Paul, Punab, Margus, Laan, Maris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834233/
https://www.ncbi.nlm.nih.gov/pubmed/36631630
http://dx.doi.org/10.1038/s41598-023-27750-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834233/
https://www.ncbi.nlm.nih.gov/pubmed/36631630
http://dx.doi.org/10.1038/s41598-023-27750-w

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