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TypeTitleAuthor(s)YearViews
Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung diseaseJannot, AS; Amiel, J; Pelet, A; Lantieri, F; Fernandez, RM; Verheij, JBGM; GarciaBarcelo, M; Arnold, S; Ceccherini, I; Borrego, S; Hofstra, RMW; Tam, PKH; Munnich, A; Chakravarti, A; ClergetDarpoux, F; Lyonnet, S2012100
 
Differential contributions of rare and common, coding and noncoding ret mutations to multifactorial hirschsprung disease liabilityEmison, 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, A2010602
 
Fine mapping of the 9q31 Hirschsprung's disease locusTang, CS; Sribudiani, Y; Miao, XP; De Vries, AR; Burzynski, G; So, MT; Leon, YY; Yip, BH; Osinga, J; Hui, KJWS; Verheij, JBGM; Cherny, SS; Tam, PKH; Sham, PC; Hofstra, RMW; GarciaBarceló, MM2010151
 
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