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Showing results 1 to 12 of 12

	Title	Author(s)	Issue Date	Views
	Association study of PHOX2B as a candidate gene for Hirschsprung's disease Journal:Gut	GarciaBarceló, M Sham, MH Lui, VCH Chen, BLS Ott, J Tam, PKH	2003	175
	Evidence for a new gene associated with Hirschsprung's disease: the PHOX2B gene Proceeding/Conference:Annual International Congress of the British Association of Paediatric Surgeons, BAPS 2002	Garcia-Barcelo, MM Sham, MH Lui, VCH Chen, BLS Ott, J Tam, PKH	2002	104
	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	99
	Hearing abnormalities in children with Hirschsprungs disease Proceeding/Conference:Annual Congress of the British Association of Paediatric Surgeons, BAPS 1999	Cheng, SWK Au, DKK Chen, BLS Tam, PKH	1999	102
	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	121
	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	164
	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 1 to 12 of 12