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Genetic defects in human azoospermia

As with many other diseases, genetic testing in human azoospermia was initially restricted to karyotype analyses (leading to diagnostic chromosome rearrangement tests for Klinefelter and other syndromes). With the advent of molecular biology in the 1980s, genetic screening was broadened to analyses...

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Detalles Bibliográficos
Autores principales: Ghieh, Farah, Mitchell, Valérie, Mandon-Pepin, Béatrice, Vialard, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477738/
https://www.ncbi.nlm.nih.gov/pubmed/31024732
http://dx.doi.org/10.1186/s12610-019-0086-6