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Linkage analysis excludes familial congenital hypothyroidism from chromosome 21.
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Genetics and Pathology. (Pediatric genetics)
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Genetics and Pathology. (Pediatric genetics)
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1999 (English)In: Genet Couns, Vol. 9, 265- p.Article in journal (Refereed) Published
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1999. Vol. 9, 265- p.
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URN: urn:nbn:se:uu:diva-51330OAI: oai:DiVA.org:uu-51330DiVA: diva2:79239
Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-14

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