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Article: Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome

TitleDetection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome
Authors
KeywordsApert syndrome
Molecular beacon
Non-invasive prenatal diagnosis
Plasma DNA
Issue Date2011
PublisherJohn Wiley & Sons Ltd. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/2252
Citation
Prenatal Diagnosis, 2011, v. 31 n. 2, p. 218-220 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/164818
ISSN
2015 Impact Factor: 3.043
2015 SCImago Journal Rankings: 1.450
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorAu, PKCen_HK
dc.contributor.authorKwok, YKYen_HK
dc.contributor.authorLeung, KYen_HK
dc.contributor.authorTang, LYFen_HK
dc.contributor.authorTang, MHYen_HK
dc.contributor.authorLau, ETen_HK
dc.date.accessioned2012-09-20T08:10:10Z-
dc.date.available2012-09-20T08:10:10Z-
dc.date.issued2011en_HK
dc.identifier.citationPrenatal Diagnosis, 2011, v. 31 n. 2, p. 218-220en_HK
dc.identifier.issn0197-3851en_HK
dc.identifier.urihttp://hdl.handle.net/10722/164818-
dc.languageengen_US
dc.publisherJohn Wiley & Sons Ltd. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/2252en_HK
dc.relation.ispartofPrenatal Diagnosisen_HK
dc.rightsPrenatal Diagnosis. Copyright © John Wiley & Sons Ltd.-
dc.subjectApert syndromeen_HK
dc.subjectMolecular beaconen_HK
dc.subjectNon-invasive prenatal diagnosisen_HK
dc.subjectPlasma DNAen_HK
dc.subject.meshAcrocephalosyndactylia - diagnosis - genetics-
dc.subject.meshDNA - blood-
dc.subject.meshPregnancy-
dc.subject.meshPrenatal Diagnosis-
dc.subject.meshReceptor, Fibroblast Growth Factor, Type 2 - genetics-
dc.titleDetection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndromeen_HK
dc.typeArticleen_HK
dc.identifier.emailTang, MHY: mhytang@hkucc.hku.hken_HK
dc.identifier.authorityTang, MHY=rp01701en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/pd.2672en_HK
dc.identifier.pmid21268044-
dc.identifier.scopuseid_2-s2.0-79251469789en_HK
dc.identifier.hkuros209005en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-79251469789&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume31en_HK
dc.identifier.issue2en_HK
dc.identifier.spage218en_HK
dc.identifier.epage220en_HK
dc.identifier.isiWOS:000287621500015-
dc.publisher.placeUnited Kingdomen_HK
dc.identifier.scopusauthoridAu, PKC=18533445100en_HK
dc.identifier.scopusauthoridKwok, YKY=8247106700en_HK
dc.identifier.scopusauthoridLeung, KY=8247106900en_HK
dc.identifier.scopusauthoridTang, LYF=12781255600en_HK
dc.identifier.scopusauthoridTang, MHY=8943401300en_HK
dc.identifier.scopusauthoridLau, ET=36006491400en_HK

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