Citations (15)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (6)
Sitthichai Panyasai, Surada Satthakarn & Sakorn Pornprasert. (2018) Complex Interaction of Hb Q-Thailand (HBA1: c.223G>C) with β-Thalassemia/Hb E (HBB: c.79G>A) Disease. Hemoglobin 42:1, pages 54-57.
Read now
Read now
Sumalee Jindadamrongwech, Noppawan Tungbuppha, Suporn Chuncharunee & Punnee Butthep. (2010) Hb Tak and Hb Q-Thailand in Thai Patients are S-Window Hemoglobin Variants Revealed by High Performance Liquid Chromatography. Hemoglobin 34:2, pages 161-164.
Read now
Read now
Dongzhi Li, Can Liao, Jian Li, Xingmei Xie & Huizhu Zhong. (2008) Association of Hb Q-Thailand with Heterozygous Hb E in a Chinese Patient. Hemoglobin 32:3, pages 319-321.
Read now
Read now
Can Liao, Jian Li & Dongzhi Li. (2008) Association of β-Thalassemia and Hb Q-Thailand Resulting in a Normal Hb A2 Value. Hemoglobin 32:5, pages 505-508.
Read now
Read now
Dongzhi Li, Can Liao, Xingmei Xie, Huizhu Zhong & Jian Li. (2007) Four Cases of Hb Q-H Disease Found in Southern China. Hemoglobin 31:1, pages 109-111.
Read now
Read now
Suthat Fucharoen & Pranee Winichagoon. (1997) Hemoglobinopathies in Southeast Asia: Molecular Biology and Clinical Medicine. Hemoglobin 21:4, pages 299-319.
Read now
Read now
Articles from other publishers (9)
Jianlong Zhuang, Na Zhang, Yuanbai Wang, Hegan Zhang, Yu Zheng, Yuying Jiang, Yingjun Xie & Dongmei Chen. (2021) Molecular Characterization Analysis of Thalassemia and Hemoglobinopathy in Quanzhou, Southeast China: A Large-Scale Retrospective Study. Frontiers in Genetics 12.
Crossref
Crossref
Neil S Harris, Mark Kavesh, Stacy G Beal, William E Winter & David H K Chui. (2021) When Hemoglobin Reported to Be A, S, and F Are Neither A, S, Nor F: A Tale of Two Patients. The Journal of Applied Laboratory Medicine 6:2, pages 543-549.
Crossref
Crossref
Xuan Shang & Xiangmin Xu. (2017) Update in the genetics of thalassemia: What clinicians need to know. Best Practice & Research Clinical Obstetrics & Gynaecology 39, pages 3-15.
Crossref
Crossref
Sanita Singsanan, Rossarin Karnpean, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Nattaya Sae-ung & Supan Fucharoen. (2010) Hemoglobin Q-Thailand related disorders: Origin, molecular, hematological and diagnostic aspects. Blood Cells, Molecules, and Diseases 45:3, pages 210-214.
Crossref
Crossref
Weidong Zheng, Yanhui Liu, Dong Chen, Kabin Rong, Yanfen Ge, Caiping Gong & Heping Chen. (2010) Complex interaction of Hb Q-Thailand and Hb E with α0-thalassemia and hereditary persistence of fetal hemoglobin in a Chinese family. Annals of Hematology 89:9, pages 883-888.
Crossref
Crossref
Min Lin, Jiao-Ren Wu, Li-Ye Yang, Hai-Ying Zou, Qian Wang & Lei Zheng. (2008) Hb Q-H disease: Two cases in a Cantonese family. Blood Cells, Molecules, and Diseases 41:3, pages 259-260.
Crossref
Crossref
Amit Kumar Mandal, Shveta Bisht, Vijay S. Bhat, Patnam Rajagopalan Krishnaswamy & Padmanabhan Balaram. (2008) Electrospray mass spectrometric characterization of hemoglobin Q (Hb Q-India) and a double mutant hemoglobin S/D in clinical samples. Clinical Biochemistry 41:1-2, pages 75-81.
Crossref
Crossref
Kanokwan Sanchaisuriya, Sunisa Chunpanich, Supan Fucharoen, Goonnapa Fucharoen, Pattara Sanchaisuriya & Yossombat Changtrakun. (2005) Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy. European Journal of Haematology 74:3, pages 221-227.
Crossref
Crossref
Fan-yi Zeng, Griffin P. Rodgers, Shu-zhen Huang, Alan N. Schechter, Mohammad Salamah, Susan Perrine & Patricia E. Berg. (1994) Sequence of the —530 region of the β-globin gene of sickle cell anemia patients with the Arabian haplotype. Human Mutation 3:2, pages 163-165.
Crossref
Crossref