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β-thalassemia intermedia mimicking β-thalassemia trait: The importance of family studies and HBB genotyping in phenotypically ambiguous cases.

Namrata SinghJasbir Kaur HiraSanjeev ChhabraReena DasAlka Rani KhadwalPrashant Sharma
Published in: International journal of laboratory hematology (2023)
Keyphrases
  • genome wide
  • sickle cell disease
  • high throughput
  • dna methylation
  • case control
  • gene expression
  • single cell