Results 1 to 5 of 5
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Chinese patients with sporadic Hirschsprung's disease are predominantly represented by a single RET haplotype.
Journal of medical genetics
B M J Publishing Group. The Journal's web site is located at
GarciaBarceló, MM; Sham, MH; Lui, VC; Chen, BL; Song, YQ; Lee, WS; Yung, SK; Romeo, G; Tam, PK2003625
Study of somatic RET gene rearrangement in sporadic Hirschsprung's disease by dual-colour fluorescence in situ hybridisation on interphase nuclei
Human Genome Meeting, Shanghai, China, 14-17 April, 2002
Lui, VCH; Corvi, R; Romeo, G; Tam, PKH200287
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
XLI VIII Annual International Congress, British Association of Paediatric Surgeons, London, 17-20 July 2001
Chen, B; Griseri, P; Lesueur, F; Ceccherini, I; Lui, VCH; Lo, CY; Romeo, G; Tam, PKH2001125
New restriction fragment length polymorphism (probe E9) reveals the highest linkage disequilibrium in Italian CF patients.
Acta Universitatis Carolinae Medica
Charles University in Prague, 1st Faculty of Medicine
Devoto, M; De Benedetti, L; Ronchetto, P; Romano, L; Romeo, G; Tsui, LC; Dean, M; Collins, F; Seia, M; Piceni Sereni, L1990150
Unusual segregation of cystic fibrosis alleles [6]
Nature Publishing Group. The Journal's web site is located at
Kitzis, A; Chomel, JC; Haliassos, A; Tesson, L; Kaplan, JC; Feingold, J; Giraud, G; Labbe, A; Dastugue, B; Dumur, V; Farriaux, JP; Roussel, P; Ferrec, C; Vidaud, M; Goossens, M; Bozon, D; Auvinet, M; Chambon, V; Andre, J; Lissens, W; Bonduelle, M; Liebaers, I; Cochaux, P; Vassart, G; Willems, P; DuckworthRaysiecki, G; Kerem, BS; Tsui, LC; Ray, PN; Krawczak, M; Schmidtke, J; Novelli, G; Dallapiccola, B; Gasparni, G; Pignatti, PP; Seia, M; Ferrari, M; Devoto, M; Romeo, G; Schwarz, M; Super, M; Ivinson, A; Read, AP; Meredith, L; Curtis, A; Williamson, R; Beaudet, AL; Feldman, GL; O'Brien, WE; Bowcock, AM; CavalliSforza, LL; Gilbert, F; Braman, J; King, MC1988220
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