norunaluwar j, azma rz, hafiza a, azlin i, zarina al, hamidah a, nor-rafeah t, endom i, danny-koh xr, noor-farisah ar, malisa my, rahimah a, and ainoon o.  (2017).  detection of beta thalassaemia mutations by multiplex amplification refractory system and gap-pcr.  - global globin 2020 challenge conference 2017.  . 

farah azima am, maizatul-husna mr, azma rz, hafiza a, azlin i, zarina al, hamidah a, noor-farisah ar, shuhaila a and ainoon o.  (2017).  the use of multiplex ligation-dependent probe amplification (mlpa) assay in detecting alpha thalassaemia gene abnormalities: comparison with multiplex pcr.  - 14th malaysian society of haematology annual scientific meeting.  . 

nor syazana, norunaluwar j, azma rz, hafiza a, azlin i, noor farisah ar, siti hawa, malisa my, zarina al, hamidah a, loh ck, azian m, ainoon o.  (2017).  concomitant inheritance of alpha-thalassaemia in beta thalassaemia major: a case report.  - global globin 2020 challence conference 2017.  . 

norunaluwar j, azma rz, hafiza a, azlin i, khairiliah ak, rusilawaty a, emida m, zarina al, hamidah a, rafeah t, farisah nar, malisa my, rahimah a, azian nam and ainoon o.  (2016).  detection of beta thalassaemia alleles: multiplex amplification refractory mutation system versus flow through hybridization kit.  - the 13th msh annual scientific meeting malaysian society of haematology.  . 

mardziah m, salwati s, azlin i, hafiza a, farisah nr, noraesah m, siti hawa aa, aizuddin ab, tumian nr, wong cl, azma rz.  (2016).  detection of t315i mutated bcr-abl in imatinib mesylate resistance chronic myeloid leukemia patients diagnosed in ukmmc.  - the 13th msh annual scientific meeting malaysian society of haematology.  . 

azlin i, azma rz, cheah fc, jubaidah p, nurulfatihah s, emida m, farisah nr, siti hawa aa, hafiza a, ainoon o.  (2016).  neonatal jaundice in g6pd-deficient females and the association with commonly occurring genetic mutations using single-nucleotide polymorphism detection via real-time pcr.  - the 13th msh annual scientific meeting malaysian society of haematology.  . 

nor khairina mohamed kamaruddin, caroline ho siew ling, faridah ahmad maulana, raja zahratul azma, azlin ithnin, hafiza alauddin, noor farisah,abdul razak, nor hidayati sardi, rafeah tumian, ainoon.  (2015).  concomitant hbh-paksé with jak2v617f mutation : case report.  - 2015 annual scientific meeting, 40th anniversary celebration of pathology advocates.  . 

norunaluwar j, khairiliah ausikhin k, rusilawaty a, azma rz, emida m, hafiza a, azlin i, zarina al, hamidah a, rafeah t,noor farisah ar, malisa my, ainoon o.  (2015).  molecular analysis of beta-globin gene mutations in ukmmc using multiplex amplification refractory mutation system and flow-through hybridization kit: a comparison of two methods.  - 2015 annual scientific meeting of the college of pathologists, academy of medicine malaysia & 40th anniversary celebration of the pathology advocates at berjaya times square hotel kuala lumpur.  . 

farisah nr, siti hawa aa, hidayati ns, norunaluwar j, aizuddin b, hamidah nh, azlin i, hafiza a, rafeah t, fadilah saw, azma rz.  (2015).  quantification of bcr-abl transcripts in chronic myeloid leukemia (cml) patients by real-time quantitative polymerase chain reaction.  - minggu penyelidikan perubatan dan kesihatan ke 17.  . 

siti hawa aa, farisah nr, hidayati ns, jubaida paraja md, nurulfatihah s, nur asma m, norunaluwar j, aizuddin ab, cheah fc, hafiza a, azma rz, azlin i.  (2015).  detection of g6pd variants among malaysian newborns with g6pd abnormalities in ukmmc by molecular testing.  - minggu penyelidikan perubatan dan kesihatan kali ke17.  . 

nh hamidah, nr farisah, rz azma, o ainoon, a hafiza, saw fadillah.  (2014).  str analysis for chimerism status of allogeneic peripheral blood stem cell transplantation.  - 2014 international congress of pathology & laboratory medicine (icpalm) & 48th malaysia-singapore congress of medicine. malaysian j pathol.  . 

madzlifah a, suziana mn, azma rz, hafiza a, azlin i, farisah nr, malisa my, hidayati ns, loh ck, hamidah a, zarina al, hamidah nh, ainoon o.  (2013).  co-inheritance of compound heterozygous hb lepore and beta-thalassaemia with single gene deletion alpha-thalassaemia: a case report.  - international conference on medical & health sciences.  . 

khamisah mg, azma rz, suria aa, hafiza a, leong cf, farisah nr, hidayati ns, malisa my, zarina al, hamidah a, loh ck, ainoon o.  (2013).  detection of homozygous haemoglobin constant spring by capillary electrophoresis method.  - xth malaysian national haematology scientific meeting.  . 

madzlifah a, suziana mn, azma rz, hafiza a, azlin i, farisah nr, malisa my, hidayati ns, loh ck, hamidah a, zarina al, hamidah nh, ainoon o.  (2013).  co-inheritance of compound heterozygous hb lepore and beta-thalassaemia with single gene deletion a-thalassaemia (-a3.7 type): a case report.  - international conference on medical and health sciences.  . 

rz azma, m zubaidah, i azlin, a hafiza, ns hidayati, nr farisah, nh hamidah, o ainoon..  (2011).  detection of partial g6pd deficiency using osmmr-d with hb normalization.  - 9th malaysian national haematology scientific meeting.  . 

azma r z, hidayati ns, farisah nr, hamidah nh, ainoon o.  (2008).  g6pd enzyme activity in normal term neonates using osmmr-d kit with haemoglobin normalization.  - the viith malaysian national haematology scientific meeting, kuala lumpur.  .