[Genetics and quaternary prevention. The example of haemochromatosis].
作者信息
Gérvas J, Pérez Fernández M
机构信息
Miembro del Comité Internacional de Clasificación de la WONCA. Canencia de la Sierra. Madrid. España.
出版信息
Aten Primaria. 2003;32(3):158-62. doi: 10.1016/s0212-6567(03)79238-5.
Abstract
摘要
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本文引用的文献
1
Hemochromatosis patients are untapped source of blood as war, shortages loom.随着战争爆发、血液短缺问题迫在眉睫，血色素沉着症患者成了尚未开发的血液来源。
JAMA. 2003 Mar 19;289(11):1364-6. doi: 10.1001/jama.289.11.1364.
2
Hereditary haemochromatosis: only 1% of adult HFEC282Y homozygotes in South Wales have a clinical diagnosis of iron overload.遗传性血色素沉着症：在南威尔士，成年HFEC282Y纯合子中只有1%有铁过载的临床诊断。
Hum Genet. 2002 Dec;111(6):538-43. doi: 10.1007/s00439-002-0824-1. Epub 2002 Sep 26.
3
Genetics and medicalisation.遗传学与医学化
BMJ. 2002 Apr 13;324(7342):863-4. doi: 10.1136/bmj.324.7342.863.
4
A comprehensive review of genetic association studies.遗传关联研究的全面综述。
Genet Med. 2002 Mar-Apr;4(2):45-61. doi: 10.1097/00125817-200203000-00002.
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Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.美国845G→A（C282Y）HFE遗传性血色素沉着症突变的外显率
Lancet. 2002 Jan 19;359(9302):211-8. doi: 10.1016/S0140-6736(02)07447-0.
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[Cascade effect: clinical, epidemiological and ethical implications].[级联效应：临床、流行病学及伦理学意义]
Med Clin (Barc). 2002 Jan 26;118(2):65-7. doi: 10.1016/s0025-7753(02)72283-5.
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MSJAMA: genetic disease, genetic testing, and the clinician.《美国医学会杂志》：遗传疾病、基因检测与临床医生
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BMJ. 1999 Aug 28;319(7209):531-2. doi: 10.1136/bmj.319.7209.531.
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