Microarray Analysis of Copy Number Variants on the Human Y Chromosome Reveals Novel and Frequent Duplications Overrepresented in Specific Haplogroups

BACKGROUND: The human Y chromosome is almost always excluded from genome-wide investigations of copy number variants (CNVs) due to its highly repetitive structure. This chromosome should not be forgotten, not only for its well-known relevance in male fertility, but also for its involvement in clinic...

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Detalles Bibliográficos
Autores principales: Johansson, Martin M., Van Geystelen, Anneleen, Larmuseau, Maarten H. D., Djurovic, Srdjan, Andreassen, Ole A., Agartz, Ingrid, Jazin, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554990/
https://www.ncbi.nlm.nih.gov/pubmed/26322892
http://dx.doi.org/10.1371/journal.pone.0137223

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554990/
https://www.ncbi.nlm.nih.gov/pubmed/26322892
http://dx.doi.org/10.1371/journal.pone.0137223

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