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1. Characterisation of the Cullin‐3 mutation that causes a severe form of familial hypertension and hyperkalaemia. Issue 10 (18th August 2015)

4. Functional characterization of common BCL11B gene desert variants suggests a lymphocyte-mediated association of BCL11B with aortic stiffness. (November 2018)

6. Quantification of FAM20A in human milk and identification of calcium metabolism proteins. Issue 24 (27th December 2021)

7. Urinary retinol binding protein predicts renal outcome in systemic immunoglobulin light‐chain (AL) amyloidosis. (9th August 2021)