Disclosure of Duchenne muscular dystrophy after newborn screening.
作者信息
Parsons E, Bradley D, Clarke A
机构信息
Department of Medical Genetics, University of Wales College of Medicine, Cardiff.
出版信息
Arch Dis Child. 1996 Jun;74(6):550-3. doi: 10.1136/adc.74.6.550.
Abstract
摘要
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本文引用的文献
1
"Telling bad news": physicians and the disclosure of undesirable information.
Sociol Health Illn. 1988 Jun;10(2):109-32. doi: 10.1111/j.1467-9566.1988.tb00001.x.
2
Mothers' consent to screening newborn babies for disease.母亲同意对新生儿进行疾病筛查。
BMJ. 1993 Mar 27;306(6881):858-9. doi: 10.1136/bmj.306.6881.858-c.
3
Experience with screening newborns for Duchenne muscular dystrophy in Wales.威尔士新生儿杜氏肌营养不良症筛查经验。
BMJ. 1993 Feb 6;306(6874):357-60. doi: 10.1136/bmj.306.6874.357.
4
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BMJ. 1993 Feb 6;306(6874):349. doi: 10.1136/bmj.306.6874.349.
5
Determinants of parental satisfaction with disclosure of disability.父母对残疾情况披露满意度的决定因素。
Dev Med Child Neurol. 1993 Sep;35(9):816-25. doi: 10.1111/j.1469-8749.1993.tb11733.x.
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Down's syndrome: is dissatisfaction with disclosure of diagnosis inevitable?唐氏综合征：对诊断信息披露的不满是否不可避免？
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Parental reactions to loss and disappointment: the diagnosis of Down's syndrome.
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