Penerbitan SCOPUS/ERA

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. 

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. 

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. 

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. 

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, 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. 

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. 

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.