The variations in the AXIN1 gene and susceptibility to cryptorchidism

Summary Background Cryptorchidism is one of the most common congenital anomalies in newborn boys. Although the mechanism responsible for the pathophysiology of cryptorchidism has not yet been well addressed, the Wnt signaling pathway has been involved in the development of cryptorchidism. Axin1 is a...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Journal of pediatric urology 2015-06, Vol.11 (3), p.132.e1-132.e5
Hauptverfasser:	Zhou, Bin, Tang, Tielong, Chen, Peng, Pu, Yan, Ma, Mingfu, Zhang, Danyan, Li, Lianbing, Zhang, Peng, Song, Yaping, Zhang, Lin
Format:	Artikel
Sprache:	eng
Schlagworte:	Asian Continental Ancestry Group - genetics Association Axin Protein - genetics AXIN1 Case-Control Studies Child Child, Preschool China Cryptorchidism Cryptorchidism - genetics Genetic Predisposition to Disease - genetics Humans Infant Infant, Newborn Male Pediatrics Polymorphism, Single Nucleotide - genetics Polymorphisms Urology
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!