Garima Mishra

2PUBLICATIONS
2CO-AUTHORS
HaematologyMolecular evolution
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Publications (2)

|Jun 14, 2021
D--phenotype due to RHD-RHCE hybrid transcript in a case of severe haemolytic disease of newborn with anti-Rh 17(Hrₒ) antibodies.

Anila Mani, Garima Mishra, Swati Kulkarni

|Jun 05, 2020
Characterising Indian RhD variants by serological and molecular methods.

Garima Mishra, Deepti Sachan, Deepthi Krishna

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