Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Exstrophy Of The Bladder[original query] |
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Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy. European journal of medical genetics 2010 1 53 (2): 55-60. Draaken Markus, Reutter Heiko, Schramm Charlotte, Bartels Enrika, Boemers Thomas M, Ebert Anne-Karoline, Rösch Wolfgang, Schröder Annette, Stein Raimund, Moebus Susanne, Stienen Dietlinde, Hoffmann Per, Nöthen Markus M, Ludwig Micha |
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. Human molecular genetics 2014 Oct 23 (20): 5536-44. Reutter Heiko, Draaken Markus, Pennimpede Tracie, Wittler Lars, Brockschmidt Felix F, Ebert Anne-Karolin, Bartels Enrika, Rösch Wolfgang, Boemers Thomas M, Hirsch Karin, Schmiedeke Eberhard, Meesters Christian, Becker Tim, Stein Raimund, Utsch Boris, Mangold Elisabeth, Nordenskjöld Agneta, Barker Gillian, Kockum Christina Clementsson, Zwink Nadine, Holmdahl Gundula, Läckgren Göran, Jenetzky Ekkehart, Feitz Wouter F J, Marcelis Carlo, Wijers Charlotte H W, Van Rooij Iris A L M, Gearhart John P, Herrmann Bernhard G, Ludwig Michael, Boyadjiev Simeon A, Nöthen Markus M, Mattheisen Manu |
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