Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population

BACKGROUND: Genetic causes of male infertility are hypothesized to involve multiple types of mutations, from single gene defects to complex chromosome rearrangements. Recently, several recurrent X-chromosome microdeletions (located in subtelomeric region of the long arm) were reported to be associat...

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Detalles Bibliográficos
Autores principales: Chylíková, Blanka, Hrdlička, Ivan, Veselá, Kamila, Řežábek, Karel, Liška, František
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892532/
https://www.ncbi.nlm.nih.gov/pubmed/27257673
http://dx.doi.org/10.1371/journal.pone.0156102

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892532/
https://www.ncbi.nlm.nih.gov/pubmed/27257673
http://dx.doi.org/10.1371/journal.pone.0156102

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