Genetic defects in human azoospermia
Résumé Comme pour beaucoup de maladies humaines, les analyses génétiques en cas d’azoospermie étaient initialement limitées à la réalisation d’un caryotype, conduisant au diagnostic de réarrangements chromosomiques comme pour le syndrome de Klinefelter ou autres syndromes. L’avènement de la biologie...
Main Authors: | Farah Ghieh, Valérie Mitchell, Béatrice Mandon-Pepin, François Vialard |
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Format: | Article |
Language: | English |
Published: |
BMC
2019-04-01
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Series: | Basic and Clinical Andrology |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s12610-019-0086-6 |
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