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Wei-Hao Wu, Xiao-Mei Ma, Jian-Qing Huang, Qin Lai, Fu-Neng Jiang, Cui-Yun Zou, Long-Tian Chen & Lian Yu. (2022) CRISPR/Cas9 (D10A) nickase-mediated Hb CS gene editing and genetically modified fibroblast identification. Bioengineered 13:5, pages 13398-13406.
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Chedtapak Ruengdit, Pinyaphat Khamphikham, Nathawat Jinorose & Sakorn Pornprasert. (2021) Hb Bart’s Hydrops Fetalis Syndrome and Hb H Disease Caused by Deletional Chiang Rai (– –CR) α0-Thalassemia in Two Unrelated Thai Families. Hemoglobin 45:2, pages 75-79.
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Hoa Van Nguyen, Kanokwan Sanchaisuriya, Dung Nguyen, Hoa Thi Thuy Phan, Sirivara Siridamrongvattana, Pattara Sanchaisuriya, Supan Fucharoen, Goonnapa Fucharoen & Frank P. Schelp. (2013) Thalassemia and Hemoglobinopathies in Thua Thien Hue Province, Central Vietnam. Hemoglobin 37:4, pages 333-342.
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Jaruwan Tritipsombut, Kanokwan Sanchaisuriya, Prachatip Phollarp, Dalouny Bouakhasith, Pattara Sanchaisuriya, Goonnapa Fucharoen, Supan Fucharoen & Frank P. Schelp. (2012) Micromapping of Thalassemia and Hemoglobinopathies in Diferent Regions of Northeast Thailand and Vientaine, Laos People's Democratic Republic. Hemoglobin 36:1, pages 47-56.
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Pimlak Charoenkwan, Rawee Taweephon, Rattika Sae-Tung, Pattra Thanarattanakorn & Torpong Sanguansermsri. (2005) Molecular and Clinical Features of Hb H Disease in Northern Thailand. Hemoglobin 29:2, pages 133-140.
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Vip Viprakasit, Gavivann Veerakul, Kleebsabai Sanpakit, Bunchoo Pongtanakul, Worrawut Chinchang & Voravarn S. Tanphaichitr. (2004) Acute haemolytic crisis in a Thai patient with homozygous haemoglobin Constant Spring (Hb CS/CS): a case report. Annals of Tropical Paediatrics 24:4, pages 323-328.
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Articles from other publishers (5)
V. Viprakasit. (2015) α−thalassaemia: a genotype-phenotype correlation and management. ISBT Science Series 10:S1, pages 295-304.
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Kamonlak Leecharoenkiat, Wannapa Sornjai, Kornpat Khungwanmaythawee, Atchara Paemanee, Chartchai Chaichana, Sittiruk Roytrakul, Suthat Fucharoen, Saovaros Svasti & Duncan R. Smith. (2014) Comparative Plasma Protein Profiling of Hemoglobin H Disease. Disease Markers 2014, pages 1-8.
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Attawut Chaibunruang, Simaporn Prommetta, Supawadee Yamsri, Goonnapa Fucharoen, Nattaya Sae-ung, Kanokwan Sanchaisuriya & Supan Fucharoen. (2013) Molecular and hematological studies in a large cohort of α0-thalassemia in northeast Thailand: Data from a single referral center. Blood Cells, Molecules, and Diseases 51:2, pages 89-93.
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Rinini DastidarBani GajraMadhusnata De. (2011) Molecular and Hematological Characterization of Hemoglobin H Disease in the Bengali Population of Kolkata, India. Genetic Testing and Molecular Biomarkers 15:1-2, pages 93-96.
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Anna Haywood, Helene Dreau, Adele Timbs, Anna Schuh, John Old & Shirley Henderson. (2010) Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencing. Annals of Hematology 89:12, pages 1215-1221.
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