GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia. [electronic resource]

By: Contributor(s): Producer: 20121204Description: 1273-6 p. digitalISSN:
  • 1432-1076
Subject(s): Online resources: In: European journal of pediatrics vol. 171
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Publication Type: Case Reports; Journal Article

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