Screening for beta thalassaemia.
作者信息
Petrou Mary
机构信息
Haemoglobinopathy Genetics Centre, University College London, Institute of Women's Health, University College London Hospitals NHS Foundation Trust, Pathology Division 86-96 Chenies Mews London WC1E 6HX.
出版信息
Indian J Hum Genet. 2010 Jan;16(1):1-5. doi: 10.4103/0971-6866.64934.
Abstract
摘要
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本文引用的文献
1
Expenditure to treat thalassaemia: an experience at a tertiary care hospital in India.地中海贫血治疗费用：印度一家三级护理医院的经验
Iran J Public Health. 2010;39(1):78-84. Epub 2010 Mar 31.
2
Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes.印度各邦及地区β地中海贫血基因突变分析：对遗传教育、筛查及咨询项目的启示
Hugo J. 2009 Dec;3(1-4):51-62. doi: 10.1007/s11568-010-9132-3. Epub 2010 Feb 10.
3
Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India.印度北部和西部β地中海贫血特征及其他血红蛋白病的发病率
Indian J Hum Genet. 2010 Jan;16(1):16-25. doi: 10.4103/0971-6866.64941.
4
Cascade screening for beta-thalassemia: A practical approach for identifying and counseling carriers in India.β地中海贫血的串联筛查：印度识别和咨询携带者的实用方法。
Indian J Community Med. 2009 Oct;34(4):354-6. doi: 10.4103/0970-0218.58399.
5
Is NESTROFT sufficient for mass screening for beta-thalassaemia trait?NESTROFT试验用于大规模筛查β地中海贫血特征是否足够？
J Med Screen. 2007;14(4):169-73. doi: 10.1258/096914107782912086.
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Assessing the impact of screening and counselling high school children for beta-thalassaemia in India.
J Med Screen. 2007;14(3):158. doi: 10.1258/096914107782066202.
7
Premarital screening for thalassemia and sickle cell disease in Saudi Arabia.沙特阿拉伯的地中海贫血和镰状细胞病婚前筛查。
Genet Med. 2007 Jun;9(6):372-7. doi: 10.1097/gim.0b013e318065a9e8.
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FINDbase: a relational database recording frequencies of genetic defects leading to inherited disorders worldwide.FINDbase：一个记录全球导致遗传性疾病的基因缺陷发生频率的关系型数据库。
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'Rakter dosh'--corrupting blood: The challenges of preventing thalassemia in Bengal, India.“拉克特多什”——血液腐败：印度孟加拉邦预防地中海贫血的挑战。
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