Cargando…
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Classic bladder exstrophy represents the most severe end of all human congenital anomalies of the kidney and urinary tract and is associated with bladder cancer susceptibility. Previous genetic studies identified one locus to be involved in classic bladder exstrophy, but were limited to a restrict n...
Ejemplares similares
-
Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation
por: Köllges, Ricarda, et al.
Publicado: (2023) -
Epidemiologic analysis of families with isolated anorectal malformations suggests high prevalence of autosomal dominant inheritance
por: Dworschak, Gabriel C., et al.
Publicado: (2017) -
Maternal drug use and the risk of anorectal malformations: systematic review and meta-analysis
por: Zwink, Nadine, et al.
Publicado: (2018) -
Treatment Strategies and Outcome of the Exstrophy–Epispadias Complex in Germany: Data From the German CURE-Net
por: Ebert, Anne-Karoline, et al.
Publicado: (2020) -
Parental risk factors and anorectal malformations: systematic review and meta-analysis
por: Zwink, Nadine, et al.
Publicado: (2011)