Phenotype Specific Association of the TGFBR3 Locus with Nonsyndromic Cryptorchidism

Purpose Based on a genome-wide association study of testicular dysgenesis syndrome showing a possible association with TGFBR3 , we analyzed data from a larger, phenotypically restricted cryptorchidism population for potential replication of this signal. Materials and Methods We excluded samples base...

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Veröffentlicht in:	The Journal of urology 2015-05, Vol.193 (5), p.1637-1645
Hauptverfasser:	Barthold, Julia S, Wang, Yanping, Kolon, Thomas F, Kollin, Claude, Nordenskjöld, Agneta, 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, Kim, Cecilia E, Mateson, Abigail B, Robbins, Alan K, Li, Jin, Akins, Robert E, Hakonarson, Hakon, Devoto, Marcella
Format:	Artikel
Sprache:	eng
Schlagworte:	Child Child, Preschool cryptorchidism Cryptorchidism - genetics genetic association studies Humans Infant Male Medicin och hälsovetenskap Phenotype Proteoglycans - genetics Receptors, Transforming Growth Factor beta - genetics testis Urology
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