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

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. Genome wide genotyping were performed in 5...

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Veröffentlicht in:	BMC urology 2016-10, Vol.16 (1), p.62-62, Article 62
Hauptverfasser:	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:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities Cryptorchidism - genetics DNA Copy Number Variations European Continental Ancestry Group - genetics Genetic aspects Genetic disorders Genetic variation Genitourinary organs Genome-Wide Association Study Humans Male Physiological aspects Risk factors Software Urology
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