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, Y., Li, J., Kolon, T.F., Olivant Fisher, A., Figueroa, T.E., Banihani, A.H., Hagerty, J.A., Gonzalez, R., Noh, P.H., Chiavacci, R.M., Harden, K.R., Abrams, D.J., Stabley, D., Kim, C.E., Sol Church, K., Hakonarson, H., Devoto, M., Barthold, J.S.. - 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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