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100
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Projek
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molecular detection of common g6pd gene mutations using hybribio`s flow-through hybridization among g6pd deficient patients in ukmmc
16-02-2017
15-12-2018
Penyelidik Bersama
molecular diagnosis of g6pd deficiency in neonates using flow-through hybridization - a comprehensive, simultaneous molecular screening approach
27-07-2017
26-11-2018
Penyelidik Bersama
molecular characterization of unknown alpha and beta globin gene rearrangements.
01-07-2014
31-12-2017
Penyelidik Bersama
detection of common beta-globin gene mutations in malaysia using hybribio`s flow-through hybridization
15-10-2015
14-01-2016
Penyelidik Bersama
spectrum of beta-gene mutations in patients diagnosed in ukmmc
10-09-2015
09-12-2015
Penyelidik Bersama
canton and mediterranean mutations : molecular characterization of g6pd deficient newborns in ukm medical centre
09-07-2015
08-10-2015
Penyelidik Bersama
Memaparkan 1 sehingga 6 dari 6 senarai
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