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Showing results 7 to 12 of 12 < previous

	Title	Author(s)	Issue Date	Views
	Mutations of SOX10 gene in Hirschsprung's disease patients with and without Waardenburg-Shah Syndrome Proceeding/Conference:Annual International Congress of the British Association of Paediatric Surgeons, BAPS 2000	Sham, MH Chen, BLS Lui, VCH Tam, PKH	2000	103
	Novel RET mutation and single nucleotide polymorphisms (SNPs) in a three generation family with Hirschsprung's disease (HSCR) Proceeding/Conference:Annual Meeting of the Pacific Association of Pediatric Surgeons, PAPS 2003	Lui, VCH Garcia-Barcelo, MM Chen, BLS Hutson, JM Tam, PKH	2003	79
	Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung disease Journal:Clinical Chemistry	Lui, VCH Leon, TYY GarciaBarcelo, MM Ganster, RW Chen, BLS Hutson, JM Tam, PKH	2005	283
	PHOX2B gene is associated with Hirschsprung's disease Proceeding/Conference:HUGO Annual Human Genome Meeting, HGM 2002	Garcia-Barcelo, MM Sham, MH Lui, VCH Chen, BLS Ott, J Tam, PKH	2002	122
	A potential hot-spot for mutations in the RET proto-oncogene for Hirschsprung's disease Proceeding/Conference:HUGO Annual Human Genome Meeting, HGM 2002	Chen, BLS Garcia-Barcelo, MM Lui, VCH Sham, MH Tam, PKH	2002	80
	Three novel mutation in exon 3 suggest a possible hot-spot in the RET proto-oncogene for Hirschsprung's disease Proceeding/Conference:Annual International Congress of the British Association of Paediatric Surgeons, BAPS 2002	Chen, BLS Garcia-Barcelo, MM Lui, VCH Sham, MH Tam, PKH	2002	115

Showing results 7 to 12 of 12 < previous