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Article: Chinese patients with sporadic Hirschsprung's disease are predominantly represented by a single RET haplotype.

TitleChinese patients with sporadic Hirschsprung's disease are predominantly represented by a single RET haplotype.
Authors
GarciaBarceló, MMSham, MHLui, VCChen, BLSong, YQLee, WSYung, SKRomeo, GTam, PK
Issue Date2003
PublisherB M J Publishing Group. The Journal's web site is located at http://jmg.bmjjournals.com/
Citation
Journal Of Medical Genetics, 2003, v. 40 n. 11, p. e122 How to Cite?
DOI: http://dx.doi.org/10.1136/jmg.40.11.e122
Persistent Identifierhttp://hdl.handle.net/10722/42618
ISSN
1468-6244
2021 Impact Factor: 5.941
2020 SCImago Journal Rankings: 2.439
PubMed Central ID
PMC1735300

 

DC FieldValueLanguage
dc.contributor.authorGarciaBarceló, MMen_HK
dc.contributor.authorSham, MHen_HK
dc.contributor.authorLui, VCen_HK
dc.contributor.authorChen, BLen_HK
dc.contributor.authorSong, YQen_HK
dc.contributor.authorLee, WSen_HK
dc.contributor.authorYung, SKen_HK
dc.contributor.authorRomeo, Gen_HK
dc.contributor.authorTam, PKen_HK
dc.date.accessioned2007-03-23T04:27:59Z-
dc.date.available2007-03-23T04:27:59Z-
dc.date.issued2003en_HK
dc.identifier.citationJournal Of Medical Genetics, 2003, v. 40 n. 11, p. e122en_HK
dc.identifier.issn1468-6244en_HK
dc.identifier.urihttp://hdl.handle.net/10722/42618-
dc.format.extent324349 bytes-
dc.format.extent26112 bytes-
dc.format.extent145392 bytes-
dc.format.extent2010 bytes-
dc.format.extent2666 bytes-
dc.format.extent2454 bytes-
dc.format.mimetypeapplication/pdf-
dc.format.mimetypeapplication/msword-
dc.format.mimetypeapplication/pdf-
dc.format.mimetypetext/plain-
dc.languageengen_HK
dc.publisherB M J Publishing Group. The Journal's web site is located at http://jmg.bmjjournals.com/en_HK
dc.relation.ispartofJournal of medical geneticsen_HK
dc.rightsJournal of Medical Genetics. Copyright © B M J Publishing Group.en_HK
dc.subject.meshHaplotypes - geneticsen_HK
dc.subject.meshHirschsprung disease - epidemiology - ethnology - geneticsen_HK
dc.subject.meshOncogene proteins - geneticsen_HK
dc.subject.meshReceptor protein-tyrosine kinases - geneticsen_HK
dc.subject.meshPolymorphism, single nucleotide - geneticsen_HK
dc.titleChinese patients with sporadic Hirschsprung's disease are predominantly represented by a single RET haplotype.en_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0022-2593&volume=40&issue=11&spage=e122:1&epage=7&date=2003&atitle=Chinese+patients+with+sporadic+Hirschsprung%27s+disease+are+predominantly+represented+by+a+single+RET+haplotypeen_HK
dc.identifier.emailGarciaBarceló, MM: mmgarcia@hkucc.hku.hken_HK
dc.identifier.emailSham, MH: mhsham@hkucc.hku.hken_HK
dc.identifier.emailLui, VC: vchlui@hkucc.hku.hken_HK
dc.identifier.emailSong, YQ: songy@hkucc.hku.hken_HK
dc.identifier.emailTam, PK: paultam@hkucc.hku.hken_HK
dc.identifier.authorityGarciaBarceló, MM=rp00445en_HK
dc.identifier.authoritySham, MH=rp00380en_HK
dc.identifier.authorityLui, VC=rp00363en_HK
dc.identifier.authoritySong, YQ=rp00488en_HK
dc.identifier.authorityTam, PK=rp00060en_HK
dc.description.naturepublished_or_final_versionen_HK
dc.identifier.doi10.1136/jmg.40.11.e122en_HK
dc.identifier.pmid14627689-
dc.identifier.pmcidPMC1735300-
dc.identifier.scopuseid_2-s2.0-1542438600en_HK
dc.identifier.hkuros88342-
dc.identifier.volume40en_HK
dc.identifier.issue11en_HK
dc.identifier.spagee122en_HK
dc.identifier.epagee122en_HK
dc.identifier.scopusauthoridGarciaBarceló, MM=6701767303en_HK
dc.identifier.scopusauthoridSham, MH=7003729109en_HK
dc.identifier.scopusauthoridLui, VC=7004231344en_HK
dc.identifier.scopusauthoridChen, BL=7408607939en_HK
dc.identifier.scopusauthoridSong, YQ=7404921212en_HK
dc.identifier.scopusauthoridLee, WS=7407084160en_HK
dc.identifier.scopusauthoridYung, SK=7006540968en_HK
dc.identifier.scopusauthoridRomeo, G=7202071987en_HK
dc.identifier.scopusauthoridTam, PK=7202539421en_HK
dc.identifier.issnl0022-2593-

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