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Conference Paper: Report of a joint WHO/WFH meeting on the control of haemophilia: Carrier detection and prenatal diagnosis

TitleReport of a joint WHO/WFH meeting on the control of haemophilia: Carrier detection and prenatal diagnosis
Authors
Issue Date1993
PublisherLippincott Williams & Wilkins. The Journal's web site is located at http://www.bloodcoagulation.com
Citation
Blood Coagulation And Fibrinolysis, 1993, v. 4 n. 2, p. 313-344 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/163539
ISSN
2015 Impact Factor: 1.242
2015 SCImago Journal Rankings: 0.496
ISI Accession Number ID

 

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.contributor.authorTuddenham, EGDen_US
dc.date.accessioned2012-09-05T05:37:13Z-
dc.date.available2012-09-05T05:37:13Z-
dc.date.issued1993en_US
dc.identifier.citationBlood Coagulation And Fibrinolysis, 1993, v. 4 n. 2, p. 313-344en_US
dc.identifier.issn0957-5235en_US
dc.identifier.urihttp://hdl.handle.net/10722/163539-
dc.languageengen_US
dc.publisherLippincott Williams & Wilkins. The Journal's web site is located at http://www.bloodcoagulation.comen_US
dc.relation.ispartofBlood Coagulation and Fibrinolysisen_US
dc.subject.meshBase Sequenceen_US
dc.subject.meshGene Therapyen_US
dc.subject.meshGenetic Linkageen_US
dc.subject.meshHemophilia A - Diagnosis - Genetics - Prevention & Controlen_US
dc.subject.meshHeterozygoteen_US
dc.subject.meshHeterozygote Detectionen_US
dc.subject.meshHumansen_US
dc.subject.meshMolecular Sequence Dataen_US
dc.subject.meshPedigreeen_US
dc.subject.meshPhenotypeen_US
dc.subject.meshPrenatal Diagnosisen_US
dc.subject.meshWorld Health Organizationen_US
dc.titleReport of a joint WHO/WFH meeting on the control of haemophilia: Carrier detection and prenatal diagnosisen_US
dc.typeConference_Paperen_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.doi10.1097/00001721-199304000-00013-
dc.identifier.pmid8185729-
dc.identifier.scopuseid_2-s2.0-0027476576en_US
dc.identifier.volume4en_US
dc.identifier.issue2en_US
dc.identifier.spage313en_US
dc.identifier.epage344en_US
dc.identifier.isiWOS:A1993KV76600013-
dc.publisher.placeUnited Statesen_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.scopusauthoridTuddenham, EGD=7005950243en_US

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