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Article: Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.

TitleSpectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.
Authors
Lam, CWYeung, WLKo, CHPoon, PMTong, SFChan, KYLo, IFChan, LYHui, JWong, VPang, CPLo, YMFok, TF
Issue Date2000
PublisherB M J Publishing Group. The Journal's web site is located at http://jmg.bmjjournals.com/
Citation
Journal Of Medical Genetics, 2000, v. 37 n. 12, p. E41 How to Cite?
DOI: http://dx.doi.org/10.1136/jmg.37.12.e41
Persistent Identifierhttp://hdl.handle.net/10722/42428
ISSN
1468-6244
2021 Impact Factor: 5.941
2020 SCImago Journal Rankings: 2.439
PubMed Central ID
PMC1734495

 

DC FieldValueLanguage
dc.contributor.authorLam, CWen_HK
dc.contributor.authorYeung, WLen_HK
dc.contributor.authorKo, CHen_HK
dc.contributor.authorPoon, PMen_HK
dc.contributor.authorTong, SFen_HK
dc.contributor.authorChan, KYen_HK
dc.contributor.authorLo, IFen_HK
dc.contributor.authorChan, LYen_HK
dc.contributor.authorHui, Jen_HK
dc.contributor.authorWong, Ven_HK
dc.contributor.authorPang, CPen_HK
dc.contributor.authorLo, YMen_HK
dc.contributor.authorFok, TFen_HK
dc.date.accessioned2007-01-29T08:49:45Z-
dc.date.available2007-01-29T08:49:45Z-
dc.date.issued2000en_HK
dc.identifier.citationJournal Of Medical Genetics, 2000, v. 37 n. 12, p. E41en_HK
dc.identifier.issn1468-6244en_HK
dc.identifier.urihttp://hdl.handle.net/10722/42428-
dc.format.extent131192 bytes-
dc.format.extent25600 bytes-
dc.format.mimetypeapplication/pdf-
dc.format.mimetypeapplication/msword-
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.meshChromosomal proteins, non-histoneen_HK
dc.subject.meshCodon, nonsenseen_HK
dc.subject.meshAutistic disorder - geneticsen_HK
dc.subject.meshAsian continental ancestry group -geneticsen_HK
dc.subject.meshDna-binding proteins - geneticsen_HK
dc.titleSpectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.en_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0022-2593&volume=37&issue=12&spage=e41:1&epage=4&date=2000&atitle=Spectrum+of+mutations+in+the+MECP2+gene+in+patients+with+infantile+autism+and+Rett+syndromeen_HK
dc.identifier.emailLam, CW:ching-wanlam@pathology.hku.hken_HK
dc.identifier.emailWong, V:vcnwong@hku.hken_HK
dc.identifier.authorityLam, CW=rp00260en_HK
dc.identifier.authorityWong, V=rp00334en_HK
dc.description.naturepublished_or_final_versionen_HK
dc.identifier.doi10.1136/jmg.37.12.e41en_HK
dc.identifier.pmid11106359-
dc.identifier.pmcidPMC1734495-
dc.identifier.scopuseid_2-s2.0-0034540747en_HK
dc.identifier.hkuros64195-
dc.identifier.volume37en_HK
dc.identifier.issue12en_HK
dc.identifier.spageE41en_HK
dc.identifier.epageE41en_HK
dc.identifier.scopusauthoridLam, CW=34570692600en_HK
dc.identifier.scopusauthoridYeung, WL=7102370747en_HK
dc.identifier.scopusauthoridKo, CH=26651291700en_HK
dc.identifier.scopusauthoridPoon, PM=7101925989en_HK
dc.identifier.scopusauthoridTong, SF=7201486672en_HK
dc.identifier.scopusauthoridChan, KY=37013153800en_HK
dc.identifier.scopusauthoridLo, IF=7004438286en_HK
dc.identifier.scopusauthoridChan, LY=8108378300en_HK
dc.identifier.scopusauthoridHui, J=7102160023en_HK
dc.identifier.scopusauthoridWong, V=7202525632en_HK
dc.identifier.scopusauthoridPang, CP=7201425127en_HK
dc.identifier.scopusauthoridLo, YM=7401935391en_HK
dc.identifier.scopusauthoridFok, TF=7006455238en_HK
dc.identifier.issnl0022-2593-

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