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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/6964
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dc.contributor.authorSmith, A.-
dc.contributor.authorEgan, J.-
dc.contributor.authorRidley, G.-
dc.contributor.authorHaan, E.-
dc.contributor.authorMontgomery, P.-
dc.contributor.authorWilliams, K.-
dc.contributor.authorElliott, E.-
dc.date.issued2003-
dc.identifier.citationArchives of Disease in Childhood, 2003; 88(3):263-264-
dc.identifier.issn0003-9888-
dc.identifier.issn1468-2044-
dc.identifier.urihttp://hdl.handle.net/2440/6964-
dc.description.abstractThis is the first population based study to estimate the birth prevalence of DNA proven Prader-Willi syndrome. Thirty infants were reported to the Australian Paediatric Surveillance Unit between 1998 and 2000, a prevalence of 4 per 100 000 live births or ~1/25 000 live births per annum.-
dc.description.statementofresponsibilityA Smith, J Egan, G Ridley, E Haan, P Montgomery, K Williams, E Elliott-
dc.language.isoen-
dc.publisherBritish Med Journal Publ Group-
dc.rightsCopyright © 2003 by the BMJ Publishing Group Ltd.-
dc.source.urihttp://dx.doi.org/10.1136/adc.88.3.263-
dc.subjectPrader-Willi syndrome-
dc.subjectgenetics-
dc.subjectepidemiology-
dc.titleBirth prevalence of Prader-Willi syndrome in Australia-
dc.typeJournal article-
dc.identifier.doi10.1136/adc.88.3.263-
pubs.publication-statusPublished-
dc.identifier.orcidHaan, E. [0000-0002-7310-5124]-
Appears in Collections:Aurora harvest 5
Paediatrics publications

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