Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Abnormalities and HBB[original query] |
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Genetic basis of persistent red blood cell microcytosis in the Chinese unexplained by phenotypical testing. Journal of clinical pathology 2015 Jan 68 (1): 69-72. So Chi-Chiu, Liu Ada K, Tsang Mandy H, Ngai Donna Y, Leung Kin-Sang, Chan Amy |
Newborn Screening for Hemoglobinopathies and Red Cell Enzymopathies in Tripura State: A Malaria-Endemic State in Northeast India. Hemoglobin 2018 2 42 (1): 43-46. Upadhye Dipti, Das Rajat S, Ray Jayanta, Acharjee Shukdeb, Ghosh Kanjaksha, Colah Roshan B, Mukherjee Malay |
Hb S (HBB: c.20A>T) and ?- and ?-Thalassemia Coinheritance in Iranian Patients. Hemoglobin 2020 5 44 (2): 109-112. Azarkeivan Azita, Cohan Nader, Niazkar Hamid Reza, Azizi Arsalan, Rad Fari |
Clinical Severity of ?-Thalassemia Pediatric Patients in Myanmar. Hemoglobin 2022 8 46 (1): 66-70. Khaing Aye Aye, Myint Phyu Phyu, Paiboonsukwong Kittiphong, Win Ne, Fucharoen Suthat, Sripichai Orap |
A Rare Case of Abnormal Hemoglobin Variant Hb Mizuho: [HBB: c.206T?>?C ? 68(E12) Leu-Pro]: A First Report in the Chinese Population. Hemoglobin 2023 7 1-5. Ya-Ping Chen, Peng Wu, Heng Wang, Jiang-Fen Wu, Dan Xie, Lei Wang, Bangquan An, Shengwen Hua |
First Report of Filipino ?-Thalassemia/?-Thalassemia in a Chinese Family. Hemoglobin 2024 1 1-5. Meihuan Chen, Aixiang Lv, Siwen Zhang, Junhao Zheng, Min Zhang, Lingji Chen, Qianqian He, Jianlong Zhuang, Na Lin, Liangpu Xu, Hailong Hua |
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