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Projek	Tempoh	Peranan
molecular detection of common g6pd gene mutations using hybribio`s flow-through hybridization among g6pd deficient patients in ukmmc	16-02-201715-12-2018	Penyelidik Bersama
molecular diagnosis of g6pd deficiency in neonates using flow-through hybridization - a comprehensive, simultaneous molecular screening approach	27-07-201726-11-2018	Penyelidik Bersama
molecular characterization of unknown alpha and beta globin gene rearrangements.	01-07-201431-12-2017	Penyelidik Bersama
detection of common beta-globin gene mutations in malaysia using hybribio`s flow-through hybridization	15-10-201514-01-2016	Penyelidik Bersama
spectrum of beta-gene mutations in patients diagnosed in ukmmc	10-09-201509-12-2015	Penyelidik Bersama
canton and mediterranean mutations : molecular characterization of g6pd deficient newborns in ukm medical centre	09-07-201508-10-2015	Penyelidik Bersama

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