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You searched for: Author/Creator Sharma, Prashant

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2. Genetic basis of unexplained erythrocytosis in Indian patients. (13th June 2019)

3. A nonsense variant in the Hexokinase 1 gene (HK1) causing severe non‐spherocytic haemolytic anaemia: genetic analysis exemplifies ambiguity due to multiple Isoforms. (23rd May 2019)

6. Kilquist syndrome: A novel syndromic hearing loss disorder caused by homozygous deletion of SLC12A2. Issue 5 (12th March 2019)

7. Effect of Heavy Mass Ion (Gold) and Light Mass Ion (Boron) Irradiation on Microstructure of Tungsten. (December 2019)

8. Pan-arthropod analysis reveals somatic piRNAs as an ancestral defence against transposable elements. Issue 1 (January 2018)

10. Childhood venous thromboembolism—A careful look at complete blood count can reveal the underlying risk factor. Issue 8 (11th June 2020)