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Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3).
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Genetics and Pathology.
Department of Women's and Children's Health. (Barnneurologisk forskning/Ahlsten)
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Genetics and Pathology. (Pediatric genetics)
1999 (English)In: Am. J. Med. Genet., Vol. 82, 348- p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
1999. Vol. 82, 348- p.
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URN: urn:nbn:se:uu:diva-51329OAI: oai:DiVA.org:uu-51329DiVA: diva2:79238
Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-14

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