Craniosynostosis with ectopia lentis and a homozygous 20-base deletion in ADAMTSL4. [electronic resource]

By: Contributor(s): Producer: 20130821Description: 78-82 p. digitalISSN:
  • 1744-5094
Subject(s): Online resources: In: Ophthalmic genetics vol. 34
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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