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Tuan-Thanh Lam, Doan-Tu Nguyen, Quang Thanh Le, Duy-Anh Nguyen, Diem-Tuyet Thi Hoang, Huu Du Nguyen, Canh Chuong Nguyen, Kim Phuong Thi Doan, Nhat-Thang Tran, Thi Minh Thi Ha, Thu Huong Nhat Trinh, Van Thong Nguyen, Duc Tam Lam, Minh Tam Le, Xuan Thao Nguyen, Thu-Hang Thi Ho, Trung Hoanh Tran, Viet Thang Ho, Thanh Van Bui, Van Trong Nguyen, Phuoc Ba Hoang, Hoai Thanh Nguyen, Manh Hoan Nguyen, Thanh-Binh Vo, Duy-Khang Nguyen Le, Thao Ngoc Truong, Hong-Thuy Thi Dao, Phuong-Anh Ngoc Vo, Thien-Chi Van Nguyen, Ngoc-Nhu Thi Tran, Quynh-Nhu Thi Tran, Yen-Linh Thi Van, Thanh-Thanh Thi Nguyen, Bich-Ngoc Thi Huynh, Thanh-Phuong Thi Nguyen, Kim-Van Thi Tran, Cong-Trai Nguyen, Phuoc-Loc Doan, Thanh-Dat Nguyen, Thanh-Thuy Thi Do, Dinh-Kiet Truong, Hung Sang Tang, Ngoc-Phuong Thi Cao, Minh-Duy Phan, Hoa Giang & Hoai-Nghia Nguyen. (2022) Combined Gap-Polymerase Chain Reaction and Targeted Next-Generation Sequencing Improve α- and β-Thalassemia Carrier Screening in Pregnant Women in Vietnam. Hemoglobin 46:4, pages 233-239.
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Wittaya Jomoui, Wanicha Tepakhan, Surada Satthakarn & Sitthichai Panyasai. (2020) Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand. Scandinavian Journal of Clinical and Laboratory Investigation 80:7, pages 528-535.
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Fan Jiang, Ai-Ping Ju, Jian Li, Gui-Lan Chen, Jian-Ying Zhou, Xue-Wei Tang, Lian-Dong Zuo & Dong-Zhi Li. (2020) Hb Westmead (HBA2: c.369C>G): Hematological Characteristics in Heterozygotes with and without α0-Thalassemia. Hemoglobin 44:3, pages 153-155.
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Zeyan Zhong, Zhiyang Guan, Dina Chen, Guoxing Zhong, Hailin He, Kunxiang Yang & Jianhong Chen. (2023) Molecular analysis and clinical significance of hemoglobin Quong Sze in Huizhou city, Southern China. Taiwanese Journal of Obstetrics and Gynecology 62:5, pages 709-712.
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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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Jialong Xu, Yeru Yang, Huanbin Zhou, Xiaoxin Huang, Bizhen Chen, Nuan Chen & Yinge Wu. (2021) Cell count‐based parameters and algorithms for thalassaemia trait screening in the southern Chinese population. International Journal of Laboratory Hematology 43:4, pages 866-872.
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Zhi-Yang Guan, Ze-Yan Zhong, Hai-Lin He, Dan Chen, Guo-Xing Zhong, Kun-Xiang Yang & Jian-Hong Chen. (2021) Genetic counseling and prenatal decision for hemoglobin H disease caused by the rare α2 codon 30 (-GAG) (HBA2: c.91_93delGAG) mutation and the SEA deletion: Case series study. Taiwanese Journal of Obstetrics and Gynecology 60:4, pages 763-765.
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Ibrahim Kalle Kwaifa, Mei I. Lai & Sabariah Md Noor. (2020) Non-deletional alpha thalassaemia: a review. Orphanet Journal of Rare Diseases 15:1.
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Félix de la Fuente-Gonzalo, Jorge M. Nieto, Pilar Ricard, Javier Anguita, Rosalina Martínez, Aurea Cervera, Ana Villegas, Fernando A. González & Paloma Ropero. (2015) Hb Cervantes, Hb Marañón, Hb La Mancha and Hb Goya: Description of 4 new haemoglobinopathies. Clinical Biochemistry 48:10-11, pages 662-667.
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