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Hemoglobin
international journal for hemoglobin research
Volume 38, 2014 - Issue 4
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Research Article

A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] With Other α-Thalassemias in Malay Families

Hafiza AlauddinHaematology Unit, Department of Pathology, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysiaCorrespondence[email protected]
,
Noor-Adilah JaaparHaematology Unit, Department of Pathology, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia
,
Raja Z. AzmaHaematology Unit, Department of Pathology, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia
,
Azlin IthninHaematology Unit, Department of Pathology, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia
,
Noor-Farisah A. RazakDiagnostic Medical Laboratory Department, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia
,
C-Khai LohDepartment of Paediatrics, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia
,
Hamidah AliasDepartment of Paediatrics, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia
,
Zarina Abdul-LatiffDepartment of Paediatrics, Universiti Kebangsaan Malaysia Medical Centre Kuala LumpurMalaysia
&
Ainoon OthmanDepartment of Medical Science II, Faculty of Medicine and Health Science, Universiti Sains Islam NilaiMalaysia
 show all
Pages 277-281 | Received 01 May 2013, Accepted 11 Dec 2013, Published online: 14 May 2014

Citations (6)

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Hafiza Alauddin, Khairina Kamarudin, Tang Yee Loong, Raja Zahratul Azma, Azlin Ithnin, Norunaluwar Jalil, Noor-Farisah Razak, Danny Koh-Xuan-Rong, Endom Ismail, Loh C-Khai, Zarina Abdul Latiff, Hamidah Alias & Ainoon Othman. (2018) A Unique Interaction of IVS-I-1 (G>A) (HBA2: c.95+1G>A) with Hb Adana (HBA2: c.179G>A) Presenting as Transfusion-Dependent α-Thalassemia. Hemoglobin 42:4, pages 247-251.
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Xin Yang, Jin-Mei Yan, Jian Li, Xing-Mei Xie, Jian-Ying Zhou, Yan Li & Dong-Zhi Li. (2016) Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (– –SEA/) Deletion. Hemoglobin 40:5, pages 353-355.
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Articles from other publishers (4)

Subithira Nahanthiran, Nik Hafidzah Nik Mustapha, Subashini Chellappah Thambiah, Malina Osman, Faridah Idris & Sabariah Md Noor. (2022) Haematologic Profile of Haemoglobin Constant Spring and Its Co-inheritance With Alpha and Beta Thalassaemia Among Form Four Students in Negeri Sembilan. Malaysian Journal of Medicine and Health Sciences 18:s21, pages 23-29.
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Divashini Vijian, Wan Suriana Wan Ab Rahman, Kannan Thirumulu Ponnuraj & Zefarina Zulkafli. (2022) Clinical and Haematological Parameters of Commonly Reported Non-deletional α-thalassaemia Mutations in Southeast Asia: A Review. Malaysian Journal of Medicine and Health Sciences 18:5, pages 190-199.
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Sharon A. Singh, Susmita Sarangi, Abena Appiah-Kubi, Peihong Hsu, W. Byron Smith, Patrick G. Gallagher, Bertil Glader & David H. K. Chui. (2018) Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation. Pediatric Blood & Cancer 65:9, pages e27220.
Crossref
Jin Ai Mary Anne Tan, Siew Leng Kho, Chin Fang Ngim, Kek Heng Chua, Ai Sim Goh, Seoh Leng Yeoh & Elizabeth George. (2016) DNA studies are necessary for accurate patient diagnosis in compound heterozygosity for Hb Adana (HBA2:c.179>A) with deletional or nondeletional α-thalassaemia. Scientific Reports 6:1.
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