Long-term follow-up of a patient with 5q31.3 microdeletion syndrome and the smallest de novo 5q31.2q31.3 deletion involving PURA. [electronic resource]

By: Contributor(s): Producer: 20151120Description: 89 p. digitalISSN:
  • 1755-8166
Online resources: In: Molecular cytogenetics vol. 8
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Publication Type: Case Reports; Journal Article

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