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Deletion of chromosome 21 in a girl with congenital hypothyroidism and mild mental retardation : Molecular definition of the lesion
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Women's and Children's Health.
1996 (English)In: Am J Med Genet, Vol. 64, 501- p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
1996. Vol. 64, 501- p.
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URN: urn:nbn:se:uu:diva-52017OAI: oai:DiVA.org:uu-52017DiVA: diva2:79926
Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-15

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CiteExportLink to record
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  • apa
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