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Showing results 1 to 8 of 8

	Title	Author(s)	Issue Date
	Comparative study of RET single nucleotide polymorphism (SNP) in Chinese and Italian populations suggests ethnic variation in the genetic basis of sporadic Hirschsprung's disease Proceeding/Conference:Annual International Conference of the British Association of Paediatric Surgeons, BAPS 2001	Chen, B Griseri, P Lesueur, F Ceccherini, I Lui, VCH Lo, CY Romeo, G Tam, PKH	2001
	Differential liabilities of coding and non-coding mutations in complex disease Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2005	Burzynski, G Amiel, J Antinolo, G Borrego,, S Ceccherini, I Emison, E Eng, C Fernandez, R Garcia-Barcelo, MM Griseri, P Hofstra, R Kashuk, C Lantieri, F Lyonnet, S Tam, PKH Tullio-Pelet, A West, K Chakravarti, A	2005
	Exonic de novo mutations in sporadic Hirschsprung disease Proceeding/Conference:European Journal of Human Genetics	Hofstra, RMW Gui, H Schriemer, D Griseri, P Pelet, A Ruiz-Ferrer, M Berrios, C van Ijcken, W van den Hout, M Tam, PKH Cheng, W Tang, SM Eggen, BJL Matera, I Ceccherini, I Amiel, J Lyonnet, S Antinolo, G Borrego, S Chakravarti, A Garcia-Barcelo, MM	2014
	Higher prevalence of Hirschsprung disease in China explained by a common RET mutation Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2006	Garcia-Barcelo, MM Amiel, J Antinolo, G Borrego, S Burzynski, G Ceccherini, I Emison, E Eng, C Fernandez, R Griseri, P Hofstra, R Kashuk, C Lantien, F Lyonnet, S Miao, X Tam, PKH Tullio-Pelet, A West, K Chakravarti, A	2006
	The International Hirschsprung's Disease Consortium: differential liabiilties of coding and non-coding mutations in complex disease Proceeding/Conference:Annual International Congress of the British Association of Paediatric Suregons, BAPS 2006	Tam, PKH Garcia-Barcelo, MM Tullio-Pelet, A Lyonnet, S Lantieri, F Kashuk, C Hofstra, R Griseri, P Fernandez, R Eng, C Emison, E Burzynski, G Ceccherini, I Borrego, S Antinolo, G Amiel, J West, K Chakravarti, A	2006
	Patterns and rates of exonic de novo mutations in sporadic Hirschsprung disease patients Proceeding/Conference:European Journal of Human Genetics	Gui, H Schriemer, D Eggen, BJL Hofstra, RMW van Ijcken, W van den Hout, M Griseri, P Matera, I Ceccherini, I Pelet, A Amiel, J Lyonnet, S Garcia-Barcelo, M Tam, PKH Ruiz-Ferrer, M Antinolo, G Borrego, S Berrios, C Chakravarti, A	2013
	Population-based study of the incidence of RET mutations in Hirschsprung's disease patients Proceeding/Conference:Annual International Congress of British Association of Paediatric Surgeons	Tam, PKH Sancandi, M Costa, M Ceccherini, I Hofstra, R Chen, B Griffths, M Burge, D	1999
	Systems biology approaches to the search for disease genes in Hirschsprung‘s disease Proceeding/Conference:European Journal of Human Genetics	Luzon-Toro, B Bleda, M Fernandez, RM Garcia-Alonso, L Arnold, S Sribudiani, Y Besmond, C Lantieri, F Torroglosa, A Enguix-Riego, M Garcia-Barcelo, MM Tam, PKH Ceccherini, I Lyonnet, S Hofstra, RM Chakravarti, A Antinolo, G Dopazo, J Borrego, S	2014

Showing results 1 to 8 of 8