A maternally inherited 16p13.11‐p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features

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John Wiley & Sons Inc

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De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay

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John Wiley & Sons Inc

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Monozygotic twins with a de novo 0.32 Mb 16q24.3 deletion, including TUBB3 presenting with developmental delay and mild facial dysmorphism but without overt brain malformation

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A de novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features

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Molecular Syndromology, Vol. 5, Iss. 1, 2013-11 ,pp. : 32-35

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Interstitial 4q Deletion and Isodicentric Y-Chromosome in a Patient with Dysmorphic Features

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