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EN16q24.3 Microdeletion Syndrome
Alias:
Monosomy 16q24.3
Del(16)(q24.3)
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16q24.3 Microdeletion Syndrome, also known as monosomy 16q24.3, is related to kbg syndrome and autism spectrum disorder. An important gene associated with 16q24.3 Microdeletion Syndrome is ANKRD11 (Ankyrin Repeat Domain Containing 11). Affiliated tissues include skin, and related phenotypes are autism and protruding ear
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