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Showing results 1 to 6 of 6

	Title	Author(s)	Issue Date
	Expression of the SOX10 gene in bowel segments of normal and Hirschsprung's disease infants Proceeding/Conference:Annual Meeting of the Pacific Association of Pediatric Surgeons, PAPS 2000	Lui, VCH Fu, M Chen, BLS Sham, MH Tam, PKH	2000
	Highly Recurrent RET Mutations and Novel Mutations in Genes of the Receptor Tyrosine Kinase and Endothelin Receptor B Pathways in Chinese Patients with Sporadic Hirschsprung Disease Journal:Clinical Chemistry	GarciaBarceló, M Sham, MH Lee, WS Lui, VCH Chen, BLS Wong, KKY Wong, JSW Tam, PKH	2004
	Idiopathic slow transit constipation and megacolon are not associated with neurturin mutations Journal:Neurogastroenterology and Motility	Chen, BLS Knowles, CH Scott, M Anand, P Williams, NS Milbrandt, J Tam, PKH	2002
	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
	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
	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

Showing results 1 to 6 of 6