Cytogenic and molecular analyses of 46,XX male syndrome with clinical comparison to other groups with testicular azoospermia of genetic origin
XX male is a rare sex chromosomal disorder in infertile men. The purpose of this study was to distinguish the clinical and genetic features of the 46,XX male syndrome from other more frequent, testicular-origin azoospermic causes of male infertility. Methods: To study 46,XX male syndrome, we compare...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2013-02-01
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| coleção: | Journal of the Formosan Medical Association |
| Assuntos: | |
| Acesso em linha: | http://www.sciencedirect.com/science/article/pii/S0929664612001751 |
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