Penerbitan Lain-lain

alia suzana asri, azlin ithnin, hafiza alauddin, nor rafeah tumian, siti mariam yusuf, nozi mat zin, norunaluwar jalil, aizuddin al banna ramlee, salwati shuib, raja zahratul azma.  (2020).  concomitant bcrabl and jak2 v617f mutation in a patient with myeloproliferative neoplasm - a case report.  - 17th malaysian society of haematology scientific meeting - personalised haematology: new & the future.  67. 

alia suzana asri, raja zahratul azma, norlida mt, sharifah ms, m. hafiz, hafizah hashim, norunaluwar jalil, hafiza alauddin..  (2020).  homozygous and compound heterozygous hb malay - a case series.  - 17th malaysian society of haematology scientific meeting - personalised haematology: now and the future.  72. 

wong ying ying, hafiza alauddin,raja zahratul azma1,norunaluwar jalil, noraesah mahmud, ainoon othman.  (2019).  molecular characterization of alpha thalassaemia among secondary school students in klang valley.  - 16th msh annual scientific meeting: targeting haematology towards excellence.  122. 

nor syazana jamali, raja zahratul azma, hafiza alauddin, azlin ithnin, nor rafeah tumian, norunaluwar jalil, rinie awai, siti hawa, salwati shuib.  (2019).  bcrabl1 mutation testing in a patient with treatment failure in cml.  - the 16th annual scientific meeting, msh.  121-122. 

raja zahratul azma raja sabudin;shuhaila bt. ahmad;endom bt. ismail;zarina binti abdul latiff;siti hawa binti abu amis;hamidah binti alias;azlin binti ithnin;noor farisah binti a razak;hafiza binti alauddin;norunaluwar binti jalil;nor rafeah binti tumian;.  (2018).  molecular characterization of unknown alpha and beta globin gene rearrangements..  -

alina mf, azma rz, hafiza a, norunaluwar j, azlin i, zarina al, loh c-k, malisa my, ainoon o.  (2018).  co-inheritance of haemoglobin e with rare beta-thalassaemia cd 35 (c-a)- the other end of the spectrum of compound heterozygous hbe/ beta-thalassaemia.  - the belt and road conference on thalassaemia. 

hatta rm, azma rz, hafiza a, norunaluwar j, rafeah t, ainoon o.  (2018).  compound heterozygous hb adana with one gene deletion alpha thalassaemia in pregnancy.  - 15th annual scientific meeting malaysian society of haematology. 

alina mf, norunaluwar j, azma rz, azlin i, cheah fc, noor-farisah ar, siti-hawa aa, noor-fadzilah zulkifli and ainoon o.  (2018).  simultaneous detection of g6pd mutations by flow-through hybridization - a potential tool for genetic screening of newborn.  - 15th annual scientific meeting malaysian society of haematology, 2018. 

wong yy, azma rz, norunaluwar j, lau dsc, hafiza a..  (2018).  hb siriraj causing severe thalassaemia intermedia in compound heterozygote state.  - 15th annual scientific meeting malaysian society of haematology. 

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, 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. 

norunaluwar j, hafiza a, azlin i, azma rz, malisa my, illaina hikmah i, nurul izzah ar, and ainoon o.  (2017).  g6pd enzyme activity in normal neonates by mindray g6pd test kit on mindray bs-480.  - indian ocean rim 2017, laboratory haematology congress. 

norunaluwar j, azlin i, azma rz, hafiza a, malisa my, illaina hikmah i, nurul izzah ar, and ainoon o.  (2017).  evaluation of g6pd enzyme activity in neonates by mindray g6pd test kit on mindray bs-480.  - 14th annual scientific meeting malaysian society of haematology. 

syirah nmt, ida mi, suria aa, azma rz, azlin i, rahimah a, norunaluwar j, hamidah a, zarina al, loh ck, hafiza a..  (2017).  alpha-globin gene triplication in beta thalassaemia patients at htcm, ukmmc.  - 14th annual scientific meeting, malaysian society of haematology. 

joanna skk, farah hazirah sa, nurul najiehah nm, najatul adawiyah k, muhammad zm, norunaluwar j, maizatul husna ma, hafiza a, azlin i, raja zahratul azma rs.  (2016).  a comparative study of haematological parameters of alpha and beta thalassaemia patients diagnosed in ukm med centre.  - the 8th medical undergraduates annual scientific research meeting. 

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. 

rusilawati a, emida m, azma rz, khairiliah ak, norunaluwar j.  (2015).  detection of beta-globin gene mutations in malaysia: comparison between marms and fth methods.  - final year project presentation, uitm. 

khairiliah ak, emida m, rz azma, rusilawaty a, norunaluwar j.  (2015).  spectrum of beta gene mutations in patients diagnosed in ukmmc by using multiplex amplification refractory mutation system (marms)..  - final year project presentation, uitm. 

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. 

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. 

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. 

j norunaluwar, rz azma, i azlin, a hafiza, sn baya, m emida, o ainoon.  (2014).  rbc g6pd activity measurement - a comparison between whole blood edta sample and dried blood spot.  - 2014 international congress of pathology & laboratory medicine (icpalm) & 48th malaysia-singapore congress of medicine. 

hamidah nh, wong fl, azrena a, norun a, nor rafeah t, fadillah saw.  (2011).  detection of mpl mutation by real-time pcr assay in patients with chronic myeloproliferative neoplasma.  - the ixth malaysian national haematology scientific meeting.