Copy number variants of Ras/MAPK pathway genes in patients with isolated cryptorchidism
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DOI: 10.1111/andr.12390
Abstract: Cryptorchidism is the most common congenital disorder in boys, but the cause for most cases remains unknown. Patients with Noonan Syndrome are characterized by a typical face, growth retardation, congenital heart defects, learning disabilities and… read more here.
Keywords: cryptorchidism; copy number; isolated cryptorchidism; mapk pathway ... See more keywords