Browsing by Author Romeo, G

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Showing results 1 to 5 of 5
TitleAuthor(s)Issue DateViews
 
Chinese patients with sporadic Hirschsprung's disease are predominantly represented by a single RET haplotype.
Journal:Journal of medical genetics
GarciaBarceló, MMSham, MHLui, VCChen, BLSong, YQLee, WSYung, SKRomeo, GTam, PK
2003
 
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, BGriseri, PLesueur, FCeccherini, ILui, VCHLo, CYRomeo, GTam, PKH
2001
56
 
New restriction fragment length polymorphism (probe E9) reveals the highest linkage disequilibrium in Italian CF patients.
Journal:Acta Universitatis Carolinae Medica
Devoto, MDe Benedetti, LRonchetto, PRomano, LRomeo, GTsui, LCDean, MCollins, FSeia, MPiceni Sereni, L
1990
141
 
Study of somatic RET gene rearrangement in sporadic Hirschsprung's disease by dual-colour fluorescence in situ hybridisation on interphase nuclei
Proceeding/Conference:HUGO Annual Human Genome Meeting, HGM 2002
Lui, VCHCorvi, RRomeo, GTam, PKH
2002
 
Unusual segregation of cystic fibrosis alleles [6]
Journal:Nature
Kitzis, AChomel, JCHaliassos, ATesson, LKaplan, JCFeingold, JGiraud, GLabbe, ADastugue, BDumur, VFarriaux, JPRoussel, PFerrec, CVidaud, MGoossens, MBozon, DAuvinet, MChambon, VAndre, JLissens, WBonduelle, MLiebaers, ICochaux, PVassart, GWillems, PDuckworthRaysiecki, GKerem, BSTsui, LCRay, PNKrawczak, MSchmidtke, JNovelli, GDallapiccola, BGasparni, GPignatti, PPSeia, MFerrari, MDevoto, MRomeo, GSchwarz, MSuper, MIvinson, ARead, APMeredith, LCurtis, AWilliamson, RBeaudet, ALFeldman, GLO'Brien, WEBowcock, AMCavalliSforza, LLGilbert, FBraman, JKing, MC
1988
210
Showing results 1 to 5 of 5