Laboratory tests in the diagnosis of cystic fibrosis

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dc.contributor.authorHoffmann, M.en_ZA
dc.contributor.authorMeyer, W. P.en_ZA
dc.date.accessioned2013-07-03T08:31:40Z
dc.date.available2013-07-03T08:31:40Z
dc.date.issued2012-07
dc.descriptionPlease cite as follows: Hoffmann, M. & Meyer, W. P. 2012. Laboratory tests in the diagnosis of cystic fibrosis. CME Journal, 30(7):256-257.en_ZA
dc.descriptionThe original publication is available at http://www.cmej.org.zaen_ZA
dc.description.abstractCystic fibrosis (CF) is the most common autosomal recessive disorder among white individuals, and occurs in all South African population groups. Recent evidence suggests a prevalence of 1 in 2 000 among white South Africans and 1 in 12 000 in the coloured population. In black South Africans carrier frequency estimates have been used to project the incidence of 1 in 4 624 live births. Generally, South Africa offers diagnostic services and expertise similar to those available worldwide for CF patients.e
dc.description.versionPublishers' Versionen_ZA
dc.identifier.citationHoffmann, M. & Meyer, W. P. 2012. Laboratory tests in the diagnosis of cystic fibrosis. CME Journal, 30(7):256-257.en_ZA
dc.identifier.issn2078-5143 (online)
dc.identifier.issn0256-2170 (print)
dc.identifier.urihttp://hdl.handle.net/10019.1/83233
dc.publisherHealth & Medical Publishing Groupen_ZA
dc.rights.holderAuthors retain copyrighten_ZA
dc.subjectCystic fibrosisen_ZA
dc.subjectCystic fibrosis -- Diagnosisen_ZA
dc.titleLaboratory tests in the diagnosis of cystic fibrosisen_ZA
dc.typeArticleen_ZA
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