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Bijal Vyas

6

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KCNQ1 mutations associated with Jervell and Lange–Nielsen syndrome and autosomal recessive Romano–Ward syndrome in India—expanding the spectrum of long QT syndrome type 1

2016 American Journal of Medical Genetics Part A
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Phenotype guided characterization and molecular analysis of Indian patients with long QT syndromes.

2016 Indian pacing and electrophysiology journal
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Identification Of Mutations In Bcr-Abl Gene In Newly Diagnosed Indian Patients With Chronic Myelogenous Leukemia (CML)

2013 Blood
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