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.
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism / 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. - In: BMC UROLOGY. - ISSN 1471-2490. - 16:1(2016), p. 62. [10.1186/s12894-016-0180-4]
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism
DEVOTO, MARCELLA;
2016
Abstract
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.| File | Dimensione | Formato | |
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