Garima Mishra

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Publications (6)

• D‐‐phenotype due to RHD‐RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti‐Rh 17(Hrₒ) antibodies
  Transfusion Medicine 2021 DOI: 10.1111/tme.12799
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• Molecular characterization of RhD variant phenotypes among blood donors: A study from the coastal region of India
  Transfusion and Apheresis Science 2021 DOI: 10.1016/j.transci.2021.103142
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• Molecular characterization of a rare Rh phenotype Dc-from the Indian subcontinent
  Transfusion and Apheresis Science 2021 DOI: 10.1016/j.transci.2021.103109
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• Molecular characterization of rare D--/D-- variants in individuals of Indian origin
  Blood Transfusion 2020 DOI: 10.2450/2020.0183-20
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• Characterising Indian RhD variants by serological and molecular methods
  Transfusion Medicine 2020 DOI: 10.1111/tme.12689
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• RHD-Positive Alleles among D- C/E+ Individuals from India
  Transfusion Medicine and Hemotherapy 2018 DOI: 10.1159/000479239
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