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You searched for: Author/Creator Radhakrishnan, Kottayam

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1. Diagnosis and treatment of MYH9-RD in an Australasian cohort with thrombocytopenia. (17th November 2018)

2. Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias. Issue 5 (24th February 2018)

7. Uridine treatment normalizes the congenital dyserythropoietic anemia type II‐like hematological phenotype in a patient with homozygous mutation in the CAD gene. Issue 11 (19th August 2020)