Год: 2005
Язык: Russian
Этот материал также есть на других языках: Арабский Английский Французский Испанский Китайский (упрощенный)
Автор(ы): Bruce Evatt
Формат: Документ
Having a national patient registry means being able to answer fundamental questions about the hemophilia population within a given country. This step-by-step guide outlines the basic principles of data collection, maintenance, and analysis and compares different types of registries.
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