A de novo 11q23 deletion in a patient presenting with severe ophthalmologic findings, psychomotor retardation and facial dysmorphism. [electronic resource]

By: Contributor(s): Producer: 20150922Description: 80-4 p. digitalISSN:
  • 2791-6421
Subject(s): In: The Turkish journal of pediatrics vol. 56
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Publication Type: Case Reports; Journal Article

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