Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13

<div>Microsatellite analysis and pedigree of the family. Microsatellite from X chromosome showed one of paternal origin and other of maternal origin. Microsatellite from 15 chromosome showed a deletion of D15S541, D15S11, GARB3, and D15S113 of maternal origin.</div>

Case Reports in Genetics

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Figure 4

Figure 4: Atypical Association of Angelman Syndrome and Klinefelter Syndrome in a Boy with 47,XXY Karyotype and Deletion 15q11.2-q13 