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

@inproceedings{Wang2016GenomicCN,
  title={Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism},
  author={Yanping Wang and Jin Li and Thomas F. Kolon and Alicia Olivant Fisher and T. Ernesto Figueroa and Ahmad Banihani and Jennifer A. Hagerty and Ricardo Uribe Gonz{\'a}lez and Paul H. Noh and Rosetta Chiavacci and Kisha R. Harden and Debra J. Abrams and Deborah L. Stabley and Cecilia Kim and Katia Sol-Church and Hakon Hakonarson and Marcella Devoto and Julia Spencer Barthold},
  booktitle={BMC urology},
  year={2016}
}
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 genotyping were performed in 559 cases and 1772 controls (Group 1… CONTINUE READING