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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Published in:BMC Urol
Main Authors: 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
Format: Artigo
Language:Inglês
Published: BioMed Central 2016
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5073740/
https://ncbi.nlm.nih.gov/pubmed/27769252
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12894-016-0180-4
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