Exstrophy-epispadias Complex
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Last Posted: Feb 27, 2023
- Variants in ALX4 and their association with genitourinary defects.
Chen Ching H, et al. Andrology 2020 0 (5) 1243-1255 - Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy.
Draaken Markus, et al. European journal of medical genetics 2010 0 (2) 55-60 - Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy.
Draaken Markus, et al. PLoS genetics 2015 3 (3) e1005024 - Bladder exstrophy-epispadias complex and the role of methylenetetrahydrofolate reductase C677T polymorphism: A case control study.
Raman Venkat Shankar, et al. Journal of Indian Association of Pediatric Surgeons 0 0 (1) 28-32 - WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish.
Baranowska Körberg Izabella, et al. Human molecular genetics 2015 9 (18) 5069-78 - Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.
Reutter Heiko, et al. Human molecular genetics 2014 10 (20) 5536-44 - No TAP63 promoter mutation is detected in bladder exstrophy-epispadias complex patients.
Darling T, et al. Journal of pediatric surgery 2013 12 (12) 12 - Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complex.
Qi Lihong, et al. Birth defects research. Part A, Clinical and molecular teratology 2013 12 (12) 759-63 - Insertion/deletion polymorphisms in the ?Np63 promoter are a risk factor for bladder exstrophy epispadias complex.
Wilkins S, et al. PLoS genetics 2012 12 (12) 12 - Exstrophy-epispadias complex
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