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Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha-spectrin gene defects.

Nidhi BhattJerome M LoewPatrick G GallagherNupur Mittal
Published in: Pediatric blood & cancer (2018)
Keyphrases
  • copy number
  • genome wide
  • early onset
  • genome wide identification
  • drug induced
  • dna methylation
  • genome wide analysis