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Article: Prenatal diagnosis of homozygous α thalassaemia by direct DNA analysis of uncultured amniotic fluid cells

TitlePrenatal diagnosis of homozygous α thalassaemia by direct DNA analysis of uncultured amniotic fluid cells
Authors
Chan, VGhosh, AChan, TK
Issue Date1984
Citation
British Medical Journal, 1984, v. 288 n. 6427, p. 1327-1329 How to Cite?
DOI: http://dx.doi.org/10.1136/bmj.288.6427.1327
AbstractPrenatal diagnosis of homozygous α thalassaemia was performed in eight successive patients at risk using DNA from uncultured amniotic fluid cells. The presence of α gene was determined by restriction endonuclease mapping and hybridisation with cloned α and β globin probes. This method is reliable and may be performed at 16 weeks of gestation.
Persistent Identifierhttp://hdl.handle.net/10722/161675
ISSN
0959-8146
2020 SCImago Journal Rankings: 1.831
ISI Accession Number ID
WOS:A1984SP77100007

 

DC FieldValueLanguage
dc.contributor.authorChan, Ven_US
dc.contributor.authorGhosh, Aen_US
dc.contributor.authorChan, TKen_US
dc.date.accessioned2012-09-05T05:13:46Z-
dc.date.available2012-09-05T05:13:46Z-
dc.date.issued1984en_US
dc.identifier.citationBritish Medical Journal, 1984, v. 288 n. 6427, p. 1327-1329en_US
dc.identifier.issn0959-8146en_US
dc.identifier.urihttp://hdl.handle.net/10722/161675-
dc.description.abstractPrenatal diagnosis of homozygous α thalassaemia was performed in eight successive patients at risk using DNA from uncultured amniotic fluid cells. The presence of α gene was determined by restriction endonuclease mapping and hybridisation with cloned α and β globin probes. This method is reliable and may be performed at 16 weeks of gestation.en_US
dc.languageengen_US
dc.relation.ispartofBritish Medical Journalen_US
dc.subject.meshAmniotic Fluid - Analysisen_US
dc.subject.meshAutoradiographyen_US
dc.subject.meshDna - Analysis - Geneticsen_US
dc.subject.meshDna Restriction Enzymesen_US
dc.subject.meshFemaleen_US
dc.subject.meshFetal Diseases - Diagnosis - Geneticsen_US
dc.subject.meshHomozygoteen_US
dc.subject.meshHumansen_US
dc.subject.meshNucleic Acid Hybridizationen_US
dc.subject.meshPregnancyen_US
dc.subject.meshPrenatal Diagnosis - Methodsen_US
dc.subject.meshThalassemia - Diagnosis - Geneticsen_US
dc.titlePrenatal diagnosis of homozygous α thalassaemia by direct DNA analysis of uncultured amniotic fluid cellsen_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.doi10.1136/bmj.288.6427.1327-
dc.identifier.pmid6324946-
dc.identifier.scopuseid_2-s2.0-0021234010en_US
dc.identifier.volume288en_US
dc.identifier.issue6427en_US
dc.identifier.spage1327en_US
dc.identifier.epage1329en_US
dc.identifier.isiWOS:A1984SP77100007-
dc.identifier.scopusauthoridChan, V=7202654865en_US
dc.identifier.scopusauthoridGhosh, A=7403963873en_US
dc.identifier.scopusauthoridChan, TK=7402687762en_US
dc.identifier.issnl0959-8146-

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