Chromosome anomalies in Sri Lanka. a cytogenetic profile

dc.contributor.authorJayasekara, R.en_US
dc.date.accessioned2012-01-10T07:45:48Z
dc.date.available2012-01-10T07:45:48Z
dc.date.issued1988en_US
dc.description.abstractThe spectrum of chromosome anomalies detectedin a population refrred tothe human genetics unit, faculty of medicine, Colombo, using lymphocyte culture and giemsa banding technique, is reported. The availability and usefulness of chromosome analysis and its direct application in the preventive and curative aspects of medicine is stressed. Down syndrome showed a significantly high incedence, but with an unexpectedly high frequency of trisome 21 due to non-disjunction in young parent. The possibility of the existence of other genetics or environmental factors stronger than the influence of ageing gemetic cells, which might trigger off non-disjunction in young Sri Lankans, is suggesteden_US
dc.identifier.citationThe Ceylon Journal of Medical Science31(1)pp.1-5en_US
dc.identifier.urihttps://dl.nsf.gov.lk/handle/1/7184
dc.publisherSri Lanka Medical Association. Colomboen_US
dc.subjectPathologyen_US
dc.subjectGeneticsen_US
dc.subjectChromosome abnormalitiesen_US
dc.subjectDown syndromeen_US
dc.subjectDiagnosisen_US
dc.subjectPaediatricsen_US
dc.subjectCytologyen_US
dc.titleChromosome anomalies in Sri Lanka. a cytogenetic profileen_US
dc.typeArticleen_US

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