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Article: Haemophilia: strategies for carrier detection and prenatal diagnosis.

TitleHaemophilia: strategies for carrier detection and prenatal diagnosis.
Authors
Peake, IRLillicrap, DPBoulyjenkov, VBriet, EChan, VGinter, EKKraus, EMLjung, RMannucci, PMNicolaides, K
Issue Date1993
PublisherWorld Health Organization. The Journal's web site is located at http://www.who.int/bulletin/en/
Citation
Bulletin Of The World Health Organization, 1993, v. 71 n. 3-4, p. 429-458 How to Cite?
AbstractIn 1977 WHO published in the Bulletin a Memorandum on Methods for the Detection of Haemophilia Carriers. This was produced following a WHO/WFH (World Federation of Haemophilia) Meeting of Investigators in Geneva in November 1976, and has served as a valuable reference article on the genetics of haemophilia. The analyses discussed were based on phenotypic assessment, which, at that time, was the only procedure available. The molecular biology revolution in genetics during the 1980s made enormous contributions to our understanding of the molecular basis of the haemophilias and now permits precise carrier detection and prenatal diagnosis. WHO and WFH held a joint meeting on this subject in February 1992 in Geneva. This article is the result of these discussions.
Persistent Identifierhttp://hdl.handle.net/10722/161985
ISSN
0042-9686
2023 Impact Factor: 8.4
2023 SCImago Journal Rankings: 1.703
ISI Accession Number ID
WOS:A1993LM22500020

 

DC FieldValueLanguage
dc.contributor.authorPeake, IRen_US
dc.contributor.authorLillicrap, DPen_US
dc.contributor.authorBoulyjenkov, Ven_US
dc.contributor.authorBriet, Een_US
dc.contributor.authorChan, Ven_US
dc.contributor.authorGinter, EKen_US
dc.contributor.authorKraus, EMen_US
dc.contributor.authorLjung, Ren_US
dc.contributor.authorMannucci, PMen_US
dc.contributor.authorNicolaides, Ken_US
dc.date.accessioned2012-09-05T05:16:28Z-
dc.date.available2012-09-05T05:16:28Z-
dc.date.issued1993en_US
dc.identifier.citationBulletin Of The World Health Organization, 1993, v. 71 n. 3-4, p. 429-458en_US
dc.identifier.issn0042-9686en_US
dc.identifier.urihttp://hdl.handle.net/10722/161985-
dc.description.abstractIn 1977 WHO published in the Bulletin a Memorandum on Methods for the Detection of Haemophilia Carriers. This was produced following a WHO/WFH (World Federation of Haemophilia) Meeting of Investigators in Geneva in November 1976, and has served as a valuable reference article on the genetics of haemophilia. The analyses discussed were based on phenotypic assessment, which, at that time, was the only procedure available. The molecular biology revolution in genetics during the 1980s made enormous contributions to our understanding of the molecular basis of the haemophilias and now permits precise carrier detection and prenatal diagnosis. WHO and WFH held a joint meeting on this subject in February 1992 in Geneva. This article is the result of these discussions.en_US
dc.languageengen_US
dc.publisherWorld Health Organization. The Journal's web site is located at http://www.who.int/bulletin/en/en_US
dc.relation.ispartofBulletin of the World Health Organizationen_US
dc.subject.meshBase Sequenceen_US
dc.subject.meshChilden_US
dc.subject.meshDiscriminant Analysisen_US
dc.subject.meshFactor Ix - Geneticsen_US
dc.subject.meshFactor Viii - Geneticsen_US
dc.subject.meshFemaleen_US
dc.subject.meshGenetic Techniquesen_US
dc.subject.meshHemophilia A - Diagnosis - Geneticsen_US
dc.subject.meshHeterozygote Detectionen_US
dc.subject.meshHumansen_US
dc.subject.meshInfant, Newbornen_US
dc.subject.meshMaleen_US
dc.subject.meshMolecular Sequence Dataen_US
dc.subject.meshOdds Ratioen_US
dc.subject.meshPedigreeen_US
dc.subject.meshPhenotypeen_US
dc.subject.meshPregnancyen_US
dc.subject.meshPrenatal Diagnosis - Methodsen_US
dc.titleHaemophilia: strategies for carrier detection and prenatal diagnosis.en_US
dc.typeArticleen_US
dc.identifier.emailChan, V:vnychana@hkucc.hku.hken_US
dc.identifier.authorityChan, V=rp00320en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.pmid8324863-
dc.identifier.scopuseid_2-s2.0-0027351077en_US
dc.identifier.volume71en_US
dc.identifier.issue3-4en_US
dc.identifier.spage429en_US
dc.identifier.epage458en_US
dc.identifier.isiWOS:A1993LM22500020-
dc.publisher.placeSwitzerlanden_US
dc.identifier.scopusauthoridPeake, IR=7005884711en_US
dc.identifier.scopusauthoridLillicrap, DP=7007185140en_US
dc.identifier.scopusauthoridBoulyjenkov, V=6602100723en_US
dc.identifier.scopusauthoridBriet, E=7005628449en_US
dc.identifier.scopusauthoridChan, V=7202654865en_US
dc.identifier.scopusauthoridGinter, EK=7103183365en_US
dc.identifier.scopusauthoridKraus, EM=7101811297en_US
dc.identifier.scopusauthoridLjung, R=13006804700en_US
dc.identifier.scopusauthoridMannucci, PM=36038519800en_US
dc.identifier.scopusauthoridNicolaides, K=7203078780en_US
dc.identifier.issnl0042-9686-

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