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