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EN16p13.11 Microdeletion Syndrome
Alias:
Monosomy 16p13.11
Del(16)(p13.11)
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16p13.11 Microdeletion Syndrome, also known as monosomy 16p13.11, is related to gastroesophageal reflux and cherubism. Affiliated tissues include skin and kidney, and related phenotypes are global developmental delay and delayed speech and language development
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MALACARDS
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