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	Title	Author(s)	Issue Date
	A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease Journal:PLoS Genetics	Mederer, T Schmitteckert, S Volz, J Martinez, C Roth, R Thumberger, T Eckstein, V Scheuerer, J Thoni, C Lasitschka, F Carstensen, L Gunther, P Holland-Cunz, S Hofstra, R Brosens, E Rosenfeld, JA Schaaf, CP Schriemer, D Ceccherini, I Rusmini, M Tilghman, J Luzon-Toro, B Torroglosa, A Borrego, S Tang, CSM Garcia-Barcelo, MM Tam, P Paramasivam, N Bewerunge-Hudler, M De La Torre, C Gretz, N Rappold, GA Romero, P Niesler, B McCallion, AS	2020
	Differential contributions of rare and common, coding and noncoding ret mutations to multifactorial hirschsprung disease liability Journal:American Journal of Human Genetics	Emison, ES GarciaBarcelo, M Grice, EA Lantieri, F Amiel, J Burzynski, G Fernandez, RM Hao, L Kashuk, C West, K Miao, X Tam, PKH Griseri, P Ceccherini, I Pelet, A Jannot, AS De Pontual, L HenrionCaude, A Lyonnet, S Verheij, JBGM Hofstra, RMW Antiñolo, G Borrego, S McCallion, AS Chakravarti, A	2010

Showing results 1 to 2 of 2