Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma. [electronic resource]

By: Contributor(s): Producer: 20131029Description: 285-91 p. digitalISSN:
  • 1661-8769
Online resources: In: Molecular syndromology vol. 4
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Publication Type: Case Reports; Journal Article

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