Partial iris hypoplasia in a patient with an interstitial subtelomeric 6p deletion not including the forkhead transcription factor gene FOXC1. [electronic resource]

By: Contributor(s): Producer: 20060123Description: 1169-71 p. digitalISSN:
  • 1018-4813
Subject(s): Online resources: In: European journal of human genetics : EJHG vol. 13
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Publication Type: Case Reports; Comment; Letter

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