MyJurnal - Malaysian Citation Centre

Complex chromosomal rearrangement der(5)ins(5;3)(q31;q25q29), t(3;12)(q24;p12.2) in a dysmorphic child, - a case report

Aziati Azwari Annuar; Nik Mohd Zulfikri Mat Zin; Siti Mariam Ismail; Nurul Alia Mohd Nawi; Nazihah Mohd Yunus; Iluni Hayati; Sarina Sulong; Zilfalil Alwi; Ankathil, Ravindran.

Globin gene defects in normal and borderline haemoglobin A2 levels: An IMR experience

Durar Aqilah Zamri; Lailatul Hadziyah Mohd Pauzy; Ezalia Esa; Yuslina Mat Yusoff; Nur Aisyah Aziz; Syahzuwan Hassan; Faidatul Syazlin Abdul Hamid; Zubaidah Zakaria.

Exploring the willingness for carrier screening among extended family members of a thalassaemia carrier individual: a lesson learned

Sahiratmadja, Edhyana; Maskoen, Ani Melani; Effendy, Dadang Sjarief Hidajat; Panigoro, Ramdan.

Four nucleotide deletions of exon 47 in Dystrophin gene: a case report of a Kelantanese Duchenne Muscular Dystrophy patient

Fatimah Azman; Rose Adzrianee Adnan; Norhafizah Che Abdul Razak; Rozita Abdullah; Nazihah Mohd Yunus; Sarina Sulong; Zilfalil Alwi; Sasongko, Teguh Haryo.

Isolation of peripheral blood nucleated red blood cells from β-Thalassaemia patients using CD71 magnetic activated cell sorting

Haiyuni Mohd Yassim; Ali, Heba; Rosline Hassan; Wan Zaidah Abdullah; Muhammad Farid Johan.

DNA Methylation of IGSF4 gene as an Epigenetic Modifier in HbE/β-Thalassaemia

Haiyuni Mohd Yassim; Wan Zaidah Abdullah; Muhammad Farid Johan.

Azacytidine enhances sensitivity response to imatinib in BCR/ABL positive CML cell line

Hamid Ali Nagi Al-Jamal; Wan Rohani Wan Taib; Siti Asmaa Mat Jusoh; Aziee Sudin; Muhammad Farid Johan.

Case series of homozygous and compound heterozygosity of Hb malay, the diagnostic features and transfusion requirements

Hanizah Salwa Amran; Nurimatussolehah Sarijan; Sathar, Jameela Sathar; Sabariah Md Noor.

Haemolytic Disease of Foetus and Newborn and Haemolytic Transfusion Reaction Due to Kidd antibody in Hospital Umum Sarawak, Malaysia

Irni Mohd Yasin; Narazah Mohd Yusoff; Afifah Hassan; Muhammad Masrin Md. Zahrin.

Genetic variants in HBS1L-MYB rs9399137 and rs11759553 associated with elevated HbF levels among Filipino β°-deletion carriers

Lai, Kuan Teh; Koh, Sam Yu; Shi, Min Chua; George, Elizabeth; Mei, I Lai; Wong, Lily.

Assessing knowledge about thalassemia among reproductive age population after video media education

Rakhmilla, Lulu Eva; Larasati, Ranisa; Sahiratmadja, Edhyana K; Rohmawaty, Enny; Susanah, Susi; Effendi, Sjarif Hidayat.

A pilot study on the willingness of premarital Malays on premarital thalassaemia screening

Nor Ezzati Nor Albashri; Noor Fadzilah Zulkifli; Asral Wirda Ahmad Asnawi; Zetty Nadia Mohd Zain; Rashidah Mohamed; Sathar, Jameela; Ainoon Othman.

Evaluation of heterozygous Hb E and its interaction with deletional alpha thalassaemia in Kelantan

Nur Hidayah Muhamad Yasin; Majdan Ramli; Ilunihayati Ibrahim; Rosnah Bahar; Noraesah Mahmud; Siti Shahrum Muhamed Said; Wan Norhasanah Wan Yusoff; Marini Ramli.

Association of -582 A> G HAMP-P polymorphism and iron status of Javanese β thalassaemia carriers

Widyastiti, Nyoman Suci; Notopuro, Harianto; Suharti, Catharina; Aryati, Aryati.

Von Willebrand factor profiles of the different ABO blood groups among Malay population

Rohaida Abd Rahman; Faridah Afandi; Tun Maizura Mohd Fathullah; Rafeezul Mohamed.

Detection ofXMN1-Gγ polymorphism among patients with Hbe/βeta thalassaemia in North East Malaysia

Rose Adzrianee Adnan; Nor Sarifah Hanafi; Zilfalil Alwi; Sarina Sulong.

Co-inheritance of Southeast Asian ovalocytosis and Hb e: does it affect the red blood cells indices?

Riahi, Shahrzard; Mei, I Lai; George, Elizabeth; Ida Marhainis Isahak; Faridah Idris; Sabariah Md Noor.

Hematological parameter evaluation in different types of deletional alpha-thalassemia in Hospital Universiti Sains Malaysia

Samilawati Mohd Arifin; Marini Ramli; Rosnah Bahar.

Hb E syndrome with co-inheritance of Hb H-Constant Spring and compound beta thalassaemia: a diagnostic challenge

Wan Zuhairah Wan Embong; Rosnah Bahar; Wan Zaidah Abdullah; Marini Ramli; Noor Haslina Mohd Noor; Shafini Mohamed Yusoff.

The Haemoglobin G Makassar (Codon 6 GAG>GCG) cases in Malaysia: molecular identification and characterization

Khor, Sok Fang; Ezalia Esa; Nur Aisyah Aziz; Faidatul Syazlin Abdul Hamid; Yuslina Mat Yusoff; Zubaidah Zakaria.

An alternative method for rapid detection of alpha thalassaemia variants in Malaysia using droplet digital PCR

Lee, Tze Yan; George, Elizabeth; Mei, I Lai; Ramachandran, Vasudevan; Tan, Jin Ai Mary Anne; Lai, Kuan Teh; Raudha Othman; Nor Hidayat Hussein.

Attention and executive function impairment in children with beta-thalassaemia major

Gamayani, Uni; Gartika, Popon; Meidha, Luh Putu; Cahyani, Aih; Siti Aminah Siti Aminah; Panigoro, Ramdan.

Effect of transfusion, iron chelation and splenectomy therapies in HbE/β-thalassaemia individuals in Malaysia

Lim, Wai Feng; Muniandi, Logeswaran; George, Elizabeth; Sathar, Jameela; Teh, Lai Kuan; Lai, Mei I.

A cross sectional assessment of health-related quality of life among patients with thalassaemia in Malaysia

Wan Ismahanisa Ismail; Mohamed Azmi Ahmad Hassali; Farooqui, Maryam; Saleem Fahad; Wan Rohani Wan Taib; Muhammad Nabil Fikri Roslan.

Coinheritance of beta thalassaemia (β0 Filipino) and delta variant (HbA2 Deventer) in Sabahan population: a case series

Yuslina Mat Yusoff; Syahzuwan Hassan; Nizmah Mahani Mokhri; Nur Aisyah Aziz; Faidatul Syazlin Abdul Hamid; Ezalia Esa; Rahimah Ahmad; Zubaidah Zakaria.