EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013

The molecular diagnosis of Y-chromosomal microdeletions is a common routine genetic test which is part of the diagnostic workup of azoospermic and severe oligozoospermic men. Since 1999, the European Academy of Andrology (EAA) and the European Molecular Genetics Quality Network (EMQN) have been acti...

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Detalles Bibliográficos
Autores principales: Krausz, C, Hoefsloot, L, Simoni, M, Tüttelmann, F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Review Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065365/
https://www.ncbi.nlm.nih.gov/pubmed/24357628
http://dx.doi.org/10.1111/j.2047-2927.2013.00173.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065365/
https://www.ncbi.nlm.nih.gov/pubmed/24357628
http://dx.doi.org/10.1111/j.2047-2927.2013.00173.x

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