16p13.11 microdeletion syndrome

From BugSigDB


16p13.11 microdeletion syndrome is a recently described syndrome characterized by developmental delay, microcephaly, epilepsy, short stature, facial dysmorphism and behavioral problems.
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Aliases
  • 16p13.11 microdeletion syndrome
  • Del(16)(p13.11)
  • Monosomy 16p13.11
  • monosomy 16p13.11
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