norunaluwar jalil, raja zahratul azma, hafiza alauddin, azlin ithnin, zarina abdul latiff, hamidah alias, nor rafeah tumian, noor farisah a. razak, malisa mohd yusoff and ainoon othman.  (2018).  detection of beta-globin gene deletions in high hbf level patients using multiplex ligation-dependent probe amplification (mlpa).  - 29th mimls national scientific conference.  . 

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.  . 

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..  - .  . 

ahmed maseh, azma rz, azlin i, hafiza a, tumian nr, azmi mtamil, noor farisah ar siti hawa, mz nozi and salwati shuib.  (2018).  fluorescence in situ hybridization (fish) versus real time quantitative polymerase chain reaction (qrt-pcr) for monitoring minimal residual disease (mrd) in chronic myeloid leukaemia (cml) patients on.  - 15th annual scientific meeting malaysian society of haematology.  . 

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.  . 

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.  . 

hafiza alauddin, mustafa langa, malisa mohd yusoff, raja zahratul azma raja sabudin, azlin ithnin, noor farisah abdul razak, nor hidayati sardi, noor hamidah hussin.  (2017).  detection of a-thalassaemia in neonates on cord blood and dried blood spot samples by capillary electrophoresis.  - malaysian journal of pathology.  17-23. 

tze sean khoo, wui chuen chia, s fadilah s. abdul wahid, noor farisah a razak, hafiza alauddin, raja zahratul azma raja sabudin, ainoon othman, roshida hassan, noor hamidah hussin.  (2017).  determination of a robust paired-end sequence assembler for short tandem repeat (str) sequences: a simulation-guided approach.  - international conference in medicine icim 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.  . 

raja-zahratul azma, khamisah m-gaus, suria a-aziz, hafiza alauddin, azlin ithnin, noor-farisah razak, nor-hidayati sardi, malisa mohd-yusoff, zarina a-latiff, hamidah alias, endom ismail, danny koh-xuan-rong and ainoon othman.  (2016).  detection of homozygous haemoglobin constant spring by capillary electrophoresis method..  - arc journal of hematology.  28-32. 

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.  . 

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.  . 

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.  . 

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 ot.  (2015).  concomitant hbh-pakse with jak2v617f mutation: case report.  - the malaysian journal of pathology.  196. 

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.  . 

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.  . 

azlin ithnin, jubaidah paraja, raja zahratul azma, hafiza alauddin, cheah foo choe, noor farisah abdul razak, siti hawa abu amis, siti noor baya mohd noor, ainoon othman.  (2015).  neonatal jaundice in g6pd-deficient females and the association with commonly occurring genetic mutations using single-nucleotide polymorphism detection via real-time pcr.  - malaysian journal of pathology.  198. 

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.  . 

mustafa langa, hafiza alauddin, malisa mohd yusoff, raja zahratul azma, azlin ithnin, farisah nr, nor hidayati sardi, noor hamidah hussein.  (2015).  screening of a-thalassaemia in newborns by capillary electrophoresis system on fresh and dried cord blood samples.  - malaysian journal of pathology.  197. 

raja zahratul azma, ainoon othman, hafiza alauddin, azlin ithnin, noor farisah abdul razak, nor hidayati sardi, noor hamidah hussin.  (2014).  molecular characteristic of alpha thalassaemia among patients diagnosed in ukm medical centre.  - malaysian journal of pathology.  36(1):27-32. 

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.  . 

hafiza alauddin, noor-adilah jaapar, raja z azma, azlin ithnin, noor-farisah a razak, c-khai loh, hamidah alias, zarina abdul-latiff, ainoon othman.  (2014).  a case series alpha-thalassaemia intermedia due to compound heterozygosity for hb adana with other alpha-thalassaemias in malay families..  - hemoglobin.  277 - 281. 

azma rz, siti zubaidah m, azlin i, hafiza a, nurasyikin y, nor hidayati s, noor farisah ar, noor hamidah h, ainoon o.  (2014).  detection of partial g6pd deficiency using osmmr2000-d kit with hb normalization.  - medicine and health.  11-21. 

nh hamidah, ar munirah, a hafiza, ar farisah, a shuhaila, mn norzilawati, my jamil, o ainoon.  (2014).  prenatal diagnosis of aneuploidies in amniotic fluid by multiple ligation-dependent probe amplification (mlpa) analysis.  - malaysian journal of pathology.  163-168. 

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 alpha-thalassaemia: a case report.  - international conference on medical & health sciences.  . 

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.  . 

raja zahratul azma, ainoon othman, norazlina azman, hafiza alauddin, azlin ithnin, nurasyikin yusof, noor farisah razak, nor hidayati sardi, noor hamidah hussin.  (2012).  co-inheritance of compound heterozyqous hb constant spring and a single -a3.7 gene deletion with heterozyqous db thalassaemia: a diagnostic challenge.  - malaysian journal of pathology.  34(1):57-62. 

nh hamidah, nr farisah, ab azlinda, fl wong, s das, saw fadillah, o ainoon.  (2012).  a study of jak2 (v617f) gene mutation in patients with chronic myeloproliferative disorders.  - clinica terapeutica.  163(2):109-113. 

norazlina a, azma rz, nurasyikin y, farisah nr, hidayati ns, hamidah nh, ainoon o..  (2011).  co-inheritance of compound heterozygous hb constant spring and single gene deletion alpha thalassaemia (3.7 kb type) with heterozygous delta beta thalassaemia: a case report..  - malaysian jurnal of pathology.  33(2):136. 

hamidah nh, farisah nr, hidayati ns, aidifitrina kr, azma rz, fadilllah saw, ainoon o.  (2011).  short tandem repeat (str) analysis of chimerism in allogeneic peripheral blood stem cell transplant in ukmmc kuala lumpur.  - medicine & health.  195. 

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.  . 

hafiza alauddin, noor hamidah hussin, noor farisah a razak, azlin ithnin and ainoon othman.  (2010).  a family study of hbs in a malay family by molecular analysis.  - malaysian journal of pathology.  32(2):137-141. 

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.  . 

n hamidah, n farisah, n jalil, w fei-liang, fa wahid, a othman..  (2008).  jak2 (v617f) mutations in patients with chronic myeloproliferative disorders.  - international journal of laboratory haematology.  30 (1):121-122. 

hamidah nh, farisah nr, ezalia, hidayati ns, jamil m, suhaila a, ainoon o.  (2007).  prenatal diagnosis of alpha thalassaemia in hospital ukm.  - the malaysian journal of pathology: vol 29,(a) - 24th world congress of pathology and laboratory medicine 2007.  . 

hamidah nh, farisah nr, hidayati ns, wong fl, azma rz, ainoon o.  (2007).  screening for haemoglobin constant spring mutation by real-time pcr.  - 3rd malaysia-indonesia-brunei, congress of medicine, 2007.  .