Author:
Liao Can,Li Jian,Xie Xing-Mei,Zhou Jian-Ying,Li Dong-Zhi
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine
Reference7 articles.
1. Chan AY, So CC, Ma ES, Chan LC (2007) A laboratory strategy for genotyping haemoglobin H disease in the Chinese. J Clin Pathol 60:931–934. doi: 10.1136/jcp.2006.042242
2. Chen FE, Ooi C, Ha SY, Cheung BM, Todd D, Liang R, Chan TK, Chan V (2000) Genetic and clinical features of hemoglobin H disease in Chinese patients. N Engl J Med 343:544–550. doi: 10.1056/NEJM200008243430804
3. Ma ES, Chow EY, Chan AY, Chan LC (2001) Interaction between (--SEA) alpha-thalassemia deletion and uncommon non-deletional alpha-globin gene mutations in Chinese patients. Haematologica 86:539–540
4. Li DZ, Liao C, Li J, Xie XM, Huang YN, Wu QC (2005) Hemoglobin H hydrops fetalis syndrome resulting from the association of the --SEA deletion and the αQuong Szeα mutation in a Chinese woman. Eur J Haematol 75:259–261. doi: 10.1111/j.1600-0609.2005.00493.x
5. Goossens M, Lee KY, Liebhaber SA, Kan YW (1982) Globin structural mutant α125 Leu→Pro is a novel cause of α-thalassaemia. Nature 296:864–865. doi: 10.1038/296864a0
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