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Fig. 2 | Journal of Neurodevelopmental Disorders

Fig. 2

From: Age of diagnosis for children with chromosome 15q syndromes

Fig. 2

Age at diagnosis for deletion, UBE3A variant, and uniparental disomy genetic subtypes of Angelman syndrome registry participants diagnosed between 2010 and 2021. Boxes represent the interquartile range, with the median shown as a vertical line. Whiskers extend to values close enough not to be considered outliers (within 1.5 times the interquartile range) and circles denote outliers. For display purposes, ages greater than 15 years were set equal to 15 years

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