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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...
Autores principales: | Ghieh, Farah, Mitchell, Valérie, Mandon-Pepin, Béatrice, Vialard, François |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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 |
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