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  • Title: [Cytogenetic detection of Prader-Willi syndrome in infancy].
    Author: Götz J, Krüger G, Westphal BC, Pelz L.
    Journal: Kinderarztl Prax; 1989 May; 57(5):239-43. PubMed ID: 2747122.
    Abstract:
    In the case of characteristic chromosomal deletion of chromosome 15(q11----q13) the diagnosis of the Prader-Willi syndrome can be already confirmed in early infancy as shown in our case report. In this connection cytogenetic high-resolution techniques are indispensable. Cytogenetic and clinical problems are discussed.
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