Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism

BACKGROUND: Copy number variation (CNV) is a potential contributing factor to many genetic diseases. Here we investigated the potential association of CNV with nonsyndromic cryptorchidism, the most common male congenital genitourinary defect, in a Caucasian population. METHODS: Genome wide genotypin...

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Detalles Bibliográficos
Autores principales: Wang, Yanping, Li, Jin, Kolon, Thomas F., Olivant Fisher, Alicia, Figueroa, T. Ernesto, BaniHani, Ahmad H., Hagerty, Jennifer A., Gonzalez, Ricardo, Noh, Paul H., Chiavacci, Rosetta M., Harden, Kisha R., Abrams, Debra J., Stabley, Deborah, Kim, Cecilia E., Sol-Church, Katia, Hakonarson, Hakon, Devoto, Marcella, Barthold, Julia Spencer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073740/
https://www.ncbi.nlm.nih.gov/pubmed/27769252
http://dx.doi.org/10.1186/s12894-016-0180-4

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